Variant report

Variant	esv1816779
Chromosome Location	chr22:31743711-31797094
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:930)
CpG islands
(count:797)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:930 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:31795385-31795687	K562	blood:	n/a	n/a
2	ARID3A	chr22:31794933-31795694	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:31793679-31794177	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:31746414-31746945	HepG2	liver:	n/a	n/a
5	ATF2	chr22:31795153-31795879	H1-hESC	embryonic stem cell:	n/a	chr22:31795789-31795803
6	ATF2	chr22:31743248-31743867	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr22:31743480-31743941	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr22:31795261-31795878	GM12878	blood:	n/a	chr22:31795789-31795803
9	ATF2	chr22:31743420-31744016	GM12878	blood:	n/a	n/a
10	ATF2	chr22:31795276-31795750	GM12878	blood:	n/a	n/a
11	BACH1	chr22:31795245-31795869	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr22:31742727-31743927	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr22:31796495-31796577	K562	blood:	n/a	n/a
14	BCL3	chr22:31795118-31795897	A549	lung:	n/a	chr22:31795357-31795370 chr22:31795436-31795445 chr22:31795439-31795452
15	BCLAF1	chr22:31795078-31795629	GM12878	blood:	n/a	chr22:31795357-31795370 chr22:31795436-31795445 chr22:31795439-31795452
16	BCLAF1	chr22:31795110-31796237	GM12878	blood:	n/a	chr22:31795357-31795370 chr22:31795436-31795445 chr22:31795439-31795452
17	BCLAF1	chr22:31743103-31744033	GM12878	blood:	n/a	chr22:31743466-31743479 chr22:31743289-31743302
18	BHLHE40	chr22:31795249-31795695	K562	blood:	n/a	chr22:31795344-31795360
19	BHLHE40	chr22:31795228-31795696	GM12878	blood:	n/a	chr22:31795344-31795360
20	BHLHE40	chr22:31741505-31743828	GM12878	blood:	n/a	chr22:31743287-31743303 chr22:31742497-31742513 chr22:31741619-31741635
21	BRCA1	chr22:31795262-31795829	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr22:31795287-31796195	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr22:31748014-31748050	HepG2	liver:	n/a	n/a
24	BRCA1	chr22:31795317-31795978	HepG2	liver:	n/a	n/a
25	BRCA1	chr22:31743502-31743965	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr22:31795284-31795964	GM12878	blood:	n/a	n/a
27	CBX3	chr22:31795256-31795770	K562	blood:	n/a	n/a
28	CCNT2	chr22:31795219-31795831	K562	blood:	n/a	n/a
29	CEBPB	chr22:31769760-31769954	K562	blood:	n/a	n/a
30	CEBPB	chr22:31745224-31745528	HepG2	liver:	n/a	chr22:31745385-31745396
31	CEBPB	chr22:31794897-31795169	K562	blood:	n/a	n/a
32	CEBPB	chr22:31745228-31745476	K562	blood:	n/a	chr22:31745385-31745396
33	CEBPB	chr22:31793729-31793901	HepG2	liver:	n/a	n/a
34	CEBPB	chr22:31793675-31794008	HepG2	liver:	n/a	n/a
35	CEBPB	chr22:31745225-31745501	IMR90	lung:	n/a	chr22:31745385-31745396
36	CEBPB	chr22:31781628-31781659	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr22:31793669-31793981	HepG2	liver:	n/a	n/a
38	CEBPB	chr22:31774251-31774469	IMR90	lung:	n/a	n/a
39	CEBPD	chr22:31795141-31795779	HepG2	liver:	n/a	n/a
40	CEBPD	chr22:31795111-31795469	HepG2	liver:	n/a	n/a
41	CEBPD	chr22:31795217-31795830	K562	blood:	n/a	n/a
42	CHD1	chr22:31795170-31796016	GM12878	blood:	n/a	n/a
43	CHD1	chr22:31742799-31743871	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr22:31795189-31795945	K562	blood:	n/a	n/a
45	CHD2	chr22:31789921-31790099	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr22:31741785-31743949	Hela-S3	cervix:	n/a	chr22:31742366-31742376 chr22:31742609-31742619
47	CHD2	chr22:31743460-31743983	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr22:31795210-31796112	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr22:31795191-31795941	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr22:31795234-31796124	HepG2	liver:	n/a	n/a

(count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:31794522-31794572	Caco-2	colon:	n/a
2	chr22:31795209-31795259	PANC-1	pancreas:	n/a
3	chr22:31794522-31794572	Hepatocyte	liver:	n/a
4	chr22:31796612-31796662	AG04449	skin:	fetal
5	chr22:31794522-31794572	Caco-2	colon:	n/a
6	chr22:31795209-31795259	PANC-1	pancreas:	n/a
7	chr22:31794522-31794572	Hepatocyte	liver:	n/a
8	chr22:31796612-31796662	AG04449	skin:	fetal
9	chr22:31795531-31795581	NT2-D1	testis:	n/a
10	chr22:31795524-31795574	AoSMC	blood vessel:	n/a
11	chr22:31792361-31792411	NHBE	bronchial:	n/a
12	chr22:31795209-31795259	HRCEpiC	kidney:	n/a
13	chr22:31796123-31796173	Jurkat	blood:	n/a
14	chr22:31794522-31794572	HEK293	kidney:	embryo
15	chr22:31792361-31792411	PrEC	prostate:	n/a
16	chr22:31746540-31746590	AG09319	gingival:	n/a
17	chr22:31792361-31792411	GM12892	blood:	n/a
18	chr22:31795357-31795407	BE2_C	brain:	n/a
19	chr22:31795357-31795407	BJ	skin:	n/a
20	chr22:31795209-31795259	SK-N-SH	brain:	n/a
21	chr22:31796123-31796173	MCF10A-Er-Src	breast:	n/a
22	chr22:31792361-31792411	HCT-116	colon:	n/a
23	chr22:31796123-31796173	T-47D	breast:	n/a
24	chr22:31795209-31795259	NH-A	brain:	n/a
25	chr22:31796612-31796662	HL-60	blood:	n/a
26	chr22:31795668-31795718	HRPEpiC	eye:	n/a
27	chr22:31792361-31792411	HAEpiC	amniotic membrane:	n/a
28	chr22:31796123-31796173	SK-N-MC	brain:	n/a
29	chr22:31795531-31795581	ECC-1	luminal epithelium:	n/a
30	chr22:31795209-31795259	AG09319	gingival:	n/a
31	chr22:31795303-31795353	MCF10A-Er-Src	breast:	n/a
32	chr22:31794522-31794572	HRE	kidney:	n/a
33	chr22:31795668-31795718	Hepatocyte	liver:	n/a
34	chr22:31795357-31795407	ovcar-3	ovarian:	n/a
35	chr22:31743738-31743788	IMR90	lung:	fetal
36	chr22:31795357-31795407	AoSMC	blood vessel:	n/a
37	chr22:31795524-31795574	HEEpiC	esophagus:	n/a
38	chr22:31794522-31794572	ovcar-3	ovarian:	n/a
39	chr22:31795303-31795353	HCF	heart:	n/a
40	chr22:31794522-31794572	HMEC	breast:	n/a
41	chr22:31795531-31795581	Caco-2	colon:	n/a
42	chr22:31746540-31746590	HRPEpiC	eye:	n/a
43	chr22:31795357-31795407	HCM	heart:	n/a
44	chr22:31743738-31743788	SK-N-MC	brain:	n/a
45	chr22:31795357-31795407	HCF	heart:	n/a
46	chr22:31792361-31792411	AG10803	skin:	n/a
47	chr22:31795209-31795259	BJ	skin:	n/a
48	chr22:31795303-31795353	A549	lung:	n/a
49	chr22:31795531-31795581	NHDF-neo	bronchial:	n/a
50	chr22:31796123-31796173	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr22:31686029..31689751-chr22:31793811..31797004,3	K562	blood:
2	chr22:31746827..31749730-chr22:31771450..31774509,3	MCF-7	breast:
3	chr22:31686527..31689345-chr22:31795585..31798136,2	MCF-7	breast:
4	chr22:31795756..31797975-chr6:82164220..82166358,2	MCF-7	breast:
5	chr22:31793990..31796986-chr22:31884678..31887767,3	K562	blood:
6	chr22:31738670..31747056-chr22:31790500..31799012,36	MCF-7	breast:
7	chr22:31756408..31758509-chr22:31763975..31766005,2	MCF-7	breast:
8	chr22:31737798..31746418-chr22:31793074..31801662,34	MCF-7	breast:
9	chr22:31685604..31688964-chr22:31794244..31796594,4	MCF-7	breast:
10	chr22:31784063..31789675-chr22:31793262..31796684,7	MCF-7	breast:
11	chr22:31789927..31791884-chr22:31793432..31795429,2	K562	blood:
12	chr22:31796576..31798824-chr22:32026967..32029510,2	K562	blood:
13	chr22:31743200..31743724-chr6:34204462..34205262,2	Hela-S3	cervix:
14	chr17:61043432..61045215-chr22:31745449..31748247,2	MCF-7	breast:
15	chr22:31756408..31758509-chr22:31763975..31766005,2	MCF-7	breast:
16	chr22:31795193..31796801-chr22:32026385..32029380,2	MCF-7	breast:
17	chr22:31793990..31795602-chr22:31885862..31887767,2	K562	blood:
18	chr22:31602004..31608593-chr22:31739507..31744494,7	MCF-7	breast:
19	chr10:74033244..74035559-chr22:31742440..31745127,2	MCF-7	breast:
20	chr22:31739411..31743940-chr22:31792561..31797746,12	K562	blood:
21	chr22:31684664..31691252-chr22:31735490..31744100,29	MCF-7	breast:
22	chr22:31742290..31744009-chr22:31883766..31886602,4	MCF-7	breast:
23	chr22:31737798..31746418-chr22:31793074..31801662,34	MCF-7	breast:
24	chr22:31686927..31688705-chr22:31793727..31795655,2	K562	blood:
25	chr22:31741223..31743821-chr22:31744774..31746588,4	K562	blood:
26	chr22:31740429..31742662-chr22:31772088..31774289,2	MCF-7	breast:
27	chr22:31738670..31747056-chr22:31790500..31799012,36	MCF-7	breast:
28	chr22:31741315..31744300-chr22:31752063..31756398,4	K562	blood:
29	chr22:31746827..31749730-chr22:31771450..31774509,3	MCF-7	breast:
30	chr22:31784063..31789675-chr22:31793262..31796684,7	MCF-7	breast:
31	chr22:31687347..31689011-chr22:31741919..31743859,2	K562	blood:
32	chr22:31683915..31694680-chr22:31733392..31744713,34	MCF-7	breast:
33	chr22:31740873..31743437-chr22:31763725..31765268,2	MCF-7	breast:
34	chr22:31752405..31755254-chr22:31795462..31798225,2	K562	blood:
35	chr22:31790215..31792897-chr22:31793771..31797373,3	K562	blood:
36	chr22:31696471..31699232-chr22:31743755..31746050,2	MCF-7	breast:
37	chr22:31742672..31744282-chr22:31844664..31847017,2	MCF-7	breast:
38	chr22:31739411..31743940-chr22:31792561..31797746,12	K562	blood:
39	chr22:31742234..31743209-chr22:31794906..31795433,2	MCF-7	breast:
40	chr22:31749139..31751086-chr22:31794921..31796685,2	MCF-7	breast:
41	chr22:31740831..31745371-chr22:31755753..31759335,5	MCF-7	breast:
42	chr22:31741632..31742462-chr22:31794953..31795605,3	Hela-S3	cervix:
43	chr22:31789927..31791884-chr22:31793432..31795429,2	K562	blood:
44	chr22:31742050..31743658-chr22:31769266..31771167,2	MCF-7	breast:
45	chr22:31741637..31743152-chr22:31792594..31795088,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-338P	TF binding region
PATZ1	TF binding region
DRG1	TF binding region
RNU6-338P	CpG island
PATZ1	CpG island
DRG1	CpG island
ENSG00000213888	chromatin interactions
ENSG00000168209	chromatin interactions
ENSG00000182541	chromatin interactions
ENSG00000100105	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000228839	chromatin interactions
ENSG00000241878	chromatin interactions
ENSG00000263931	chromatin interactions
ENSG00000100100	chromatin interactions
ENSG00000198089	chromatin interactions
ENSG00000206615	chromatin interactions
ENSG00000185721	chromatin interactions
ENSG00000184708	chromatin interactions

Extended variants
information (count: 1400 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1400 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563822976	chr22:31743784-31743785	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs372432785	chr22:31743819-31743820	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs113370862	chr22:31743895-31743896	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs112183393	chr22:31743915-31743916	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs532366165	chr22:31743987-31743988	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs62236171	chr22:31743999-31744000	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs73158585	chr22:31744009-31744010	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs528786030	chr22:31744015-31744016	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs377651293	chr22:31744067-31744068	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs548935472	chr22:31744069-31744070	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs5997959	chr22:31744072-31744073	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs571280150	chr22:31744074-31744075	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs191302611	chr22:31744077-31744078	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs376188485	chr22:31744129-31744130	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs79323513	chr22:31744214-31744215	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs569741171	chr22:31744260-31744261	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs538197816	chr22:31744309-31744310	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs558124044	chr22:31744338-31744339	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs150277351	chr22:31744360-31744361	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs534587746	chr22:31744365-31744366	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs112291583	chr22:31744374-31744375	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs574306644	chr22:31744387-31744388	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs574514723	chr22:31744390-31744391	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs543614714	chr22:31744434-31744435	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs557465586	chr22:31744492-31744493	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs34176633	chr22:31744502-31744503	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs58550905	chr22:31744516-31744517	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs536446631	chr22:31744612-31744613	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs370499318	chr22:31744657-31744658	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs62236172	chr22:31744667-31744668	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs79140415	chr22:31744670-31744671	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs34306999	chr22:31744671-31744672	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs74924191	chr22:31744672-31744673	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs557131209	chr22:31744682-31744683	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs577265057	chr22:31744686-31744687	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs573482653	chr22:31744695-31744696	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs138363368	chr22:31744702-31744703	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs528525219	chr22:31744714-31744715	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs4603880	chr22:31744721-31744722	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs151127874	chr22:31744733-31744734	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs181361695	chr22:31744737-31744738	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs141540691	chr22:31744751-31744752	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs564992386	chr22:31744787-31744788	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs75042792	chr22:31744790-31744791	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs186014350	chr22:31744816-31744817	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs145301346	chr22:31744844-31744845	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs371776981	chr22:31744849-31744850	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs368164870	chr22:31744868-31744869	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs551886107	chr22:31744878-31744879	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs371632466	chr22:31744893-31744894	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31738400-31743800	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr22:31738800-31743800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr22:31740000-31744200	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr22:31740600-31743800	Active TSS	Fetal Kidney	kidney
5	chr22:31741000-31743800	Active TSS	Brain Substantia Nigra	brain
6	chr22:31741000-31744000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr22:31741000-31744200	Active TSS	H9 Cell Line	embryonic stem cell
8	chr22:31741200-31743800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr22:31741200-31743800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr22:31741200-31743800	Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr22:31741200-31743800	Active TSS	iPS-18 Cell Line	embryonic stem cell
12	chr22:31741200-31743800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
13	chr22:31741200-31743800	Active TSS	Primary T killer memory cells from peripheral blood	blood
14	chr22:31741200-31743800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr22:31741200-31743800	Active TSS	Fetal Intestine Large	intestine
16	chr22:31741200-31743800	Active TSS	Gastric	stomach
17	chr22:31741200-31743800	Active TSS	Ovary	ovary
18	chr22:31741200-31743800	Active TSS	Hela-S3	cervix
19	chr22:31741200-31744000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr22:31741200-31744000	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr22:31741200-31744000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr22:31741200-31744000	Active TSS	Psoas Muscle	Psoas
23	chr22:31741200-31744200	Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr22:31741200-31744200	Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr22:31741200-31744200	Active TSS	Colon Smooth Muscle	Colon
26	chr22:31741200-31744200	Active TSS	Fetal Brain Female	brain
27	chr22:31741400-31743800	Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr22:31741400-31743800	Active TSS	Aorta	Aorta
29	chr22:31741400-31743800	Active TSS	Brain Anterior Caudate	brain
30	chr22:31741400-31743800	Active TSS	Fetal Intestine Small	intestine
31	chr22:31741400-31743800	Active TSS	Rectal Smooth Muscle	rectum
32	chr22:31741400-31743800	Active TSS	Small Intestine	intestine
33	chr22:31741400-31743800	Active TSS	Thymus	Thymus
34	chr22:31741400-31743800	Active TSS	NHLF	lung
35	chr22:31741400-31744000	Active TSS	A549	lung
36	chr22:31741600-31743800	Active TSS	Duodenum Smooth Muscle	Duodenum
37	chr22:31741600-31744200	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr22:31741800-31743800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr22:31741800-31743800	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr22:31741800-31743800	Active TSS	Left Ventricle	heart
41	chr22:31741800-31743800	Active TSS	Lung	lung
42	chr22:31742000-31743800	Active TSS	Placenta Amnion	Placenta Amnion
43	chr22:31742000-31743800	Active TSS	Right Ventricle	heart
44	chr22:31742600-31744000	Flanking Active TSS	Primary B cells from cord blood	blood
45	chr22:31742800-31743800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr22:31742800-31743800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr22:31742800-31743800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
48	chr22:31742800-31743800	Active TSS	Stomach Mucosa	stomach
49	chr22:31742800-31743800	Active TSS	GM12878-XiMat	blood
50	chr22:31742800-31743800	Flanking Active TSS	HMEC	breast

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