Variant report

Variant	nsv8344
Chromosome Location	chr8:53850872-53854509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:53853083-53853227	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:53852611-53852810	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:53851100-53851301	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:53854127-53854469	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:53854274-53854336	GM12878	blood:	n/a	n/a
6	BRCA1	chr8:53854261-53854544	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr8:53854213-53854414	HepG2	liver:	n/a	n/a
8	BRCA1	chr8:53853372-53853513	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr8:53854282-53854519	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD1	chr8:53853898-53854325	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr8:53854213-53854389	GM12878	blood:	n/a	n/a
12	CHD1	chr8:53854039-53854723	IMR90	lung:	n/a	n/a
13	CHD2	chr8:53851260-53851279	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr8:53854284-53854530	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr8:53854239-53854481	HepG2	liver:	n/a	n/a
16	CHD2	chr8:53853125-53853738	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr8:53854182-53854464	A549	lung:	n/a	n/a
18	CREB1	chr8:53852360-53853460	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr8:53853639-53854000	A549	lung:	n/a	n/a
20	CTBP2	chr8:53851626-53854473	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr8:53854240-53854390	GM12868	blood:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
22	CTCF	chr8:53854240-53854390	NHDF-neo	bronchial:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
23	CTCF	chr8:53854240-53854390	MCF-7	breast:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
24	CTCF	chr8:53853805-53853963	Medullo	brain:	n/a	chr8:53853894-53853907
25	CTCF	chr8:53852880-53853030	GM12867	blood:	n/a	n/a
26	CTCF	chr8:53853840-53853990	BE2_C	brain:	n/a	chr8:53853894-53853907
27	CTCF	chr8:53854260-53854410	AG04450	lung:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
28	CTCF	chr8:53854146-53854459	SK-N-SH_RA	brain:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
29	CTCF	chr8:53853780-53853930	GM12872	blood:	n/a	chr8:53853894-53853907
30	CTCF	chr8:53854176-53854494	ProgFib	skin:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
31	CTCF	chr8:53854260-53854410	GM06990	blood:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
32	CTCF	chr8:53854191-53854506	Gliobla	brain:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
33	CTCF	chr8:53854260-53854410	HEEpiC	esophagus:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
34	CTCF	chr8:53853780-53853930	HepG2	liver:	n/a	chr8:53853894-53853907
35	CTCF	chr8:53854300-53854450	HEK293	kidney:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
36	CTCF	chr8:53853220-53853370	GM12870	blood:	n/a	n/a
37	CTCF	chr8:53853760-53853910	GM12865	blood:	n/a	chr8:53853894-53853907
38	CTCF	chr8:53853844-53853913	HUVEC	blood vessel:	n/a	chr8:53853894-53853907
39	CTCF	chr8:53853847-53853956	GM19239	blood:	n/a	chr8:53853894-53853907
40	CTCF	chr8:53853700-53853850	RPTEC	kidney:	n/a	n/a
41	CTCF	chr8:53853740-53853890	HRE	kidney:	n/a	n/a
42	CTCF	chr8:53854320-53854470	NHLF	lung:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
43	CTCF	chr8:53854215-53854489	LNCaP	prostate:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
44	CTCF	chr8:53853620-53853770	HFF	foreskin:	n/a	n/a
45	CTCF	chr8:53852440-53852590	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr8:53854240-53854390	GM12865	blood:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
47	CTCF	chr8:53853080-53853230	HRE	kidney:	n/a	n/a
48	CTCF	chr8:53854300-53854450	GM06990	blood:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
49	CTCF	chr8:53854280-53854430	AG04449	skin:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
50	CTCF	chr8:53852906-53852974	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53853659-53853709	RPTEC	kidney:	n/a
2	chr8:53852030-53852080	NT2-D1	testis:	n/a
3	chr8:53854172-53854222	MCF-7	breast:	n/a
4	chr8:53853112-53853162	HNPCEpiC	eye:	n/a
5	chr8:53853659-53853709	RPTEC	kidney:	n/a
6	chr8:53852030-53852080	NT2-D1	testis:	n/a
7	chr8:53854172-53854222	MCF-7	breast:	n/a
8	chr8:53853112-53853162	HNPCEpiC	eye:	n/a
9	chr8:53851707-53851757	AG09319	gingival:	n/a
10	chr8:53851156-53851206	Jurkat	blood:	n/a
11	chr8:53851156-53851206	HRPEpiC	eye:	n/a
12	chr8:53851707-53851757	HL-60	blood:	n/a
13	chr8:53851156-53851206	HNPCEpiC	eye:	n/a
14	chr8:53851156-53851206	NT2-D1	testis:	n/a
15	chr8:53854172-53854222	SAEC	small airway:	n/a
16	chr8:53854495-53854545	T-47D	breast:	n/a
17	chr8:53852422-53852472	SKMC	muscle:	n/a
18	chr8:53854425-53854475	AoSMC	blood vessel:	n/a
19	chr8:53853659-53853709	AG04449	skin:	fetal
20	chr8:53852443-53852493	IMR90	lung:	fetal
21	chr8:53852184-53852234	SKMC	muscle:	n/a
22	chr8:53853112-53853162	NHDF-neo	bronchial:	n/a
23	chr8:53851707-53851757	HMEC	breast:	n/a
24	chr8:53854425-53854475	HCM	heart:	n/a
25	chr8:53852661-53852711	Caco-2	colon:	n/a
26	chr8:53851613-53851663	NHDF-neo	bronchial:	n/a
27	chr8:53851156-53851206	HRCEpiC	kidney:	n/a
28	chr8:53854172-53854222	SK-N-SH	brain:	n/a
29	chr8:53852446-53852496	SKMC	muscle:	n/a
30	chr8:53852274-53852324	HNPCEpiC	eye:	n/a
31	chr8:53854172-53854222	GM12892	blood:	n/a
32	chr8:53853604-53853654	K562	blood:	n/a
33	chr8:53853444-53853494	HRE	kidney:	n/a
34	chr8:53852443-53852493	SK-N-SH_RA	brain:	n/a
35	chr8:53852030-53852080	AG10803	skin:	n/a
36	chr8:53851613-53851663	SK-N-SH	brain:	n/a
37	chr8:53852184-53852234	AG04450	lung:	fetal
38	chr8:53852274-53852324	AG10803	skin:	n/a
39	chr8:53853112-53853162	SK-N-SH_RA	brain:	n/a
40	chr8:53852446-53852496	HCF	heart:	n/a
41	chr8:53852184-53852234	NB4	blood:	n/a
42	chr8:53853659-53853709	HRCEpiC	kidney:	n/a
43	chr8:53852274-53852324	Jurkat	blood:	n/a
44	chr8:53852422-53852472	A549	lung:	n/a
45	chr8:53852184-53852234	NHBE	bronchial:	n/a
46	chr8:53853444-53853494	HMEC	breast:	n/a
47	chr8:53853444-53853494	HCPEpiC	choroid plexus:	n/a
48	chr8:53852446-53852496	HRCEpiC	kidney:	n/a
49	chr8:53854172-53854222	RPTEC	kidney:	n/a
50	chr8:53852443-53852493	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:53627445..53629464-chr8:53852538..53854621,2	MCF-7	breast:
2	chr8:53649395..53650276-chr8:53853945..53854772,3	MCF-7	breast:
3	chr8:53649371..53650945-chr8:53853868..53854778,6	MCF-7	breast:
4	chr8:53711623..53712255-chr8:53854248..53854877,2	MCF-7	breast:

Variant related genes	Relation type
NPBWR1	TF binding region
NPBWR1	CpG island

Extended variants
information (count: 172 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:172 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539323996	chr8:53850872-53850873	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs540634492	chr8:53850923-53850924	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs370092201	chr8:53850973-53850974	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs557944618	chr8:53850974-53850975	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs552126612	chr8:53850991-53850992	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs575817149	chr8:53851010-53851011	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs11993317	chr8:53851048-53851049	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs555040077	chr8:53851112-53851113	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs79012707	chr8:53851114-53851115	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs75536836	chr8:53851204-53851205	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs541031588	chr8:53851240-53851241	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs559041071	chr8:53851255-53851256	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs117325834	chr8:53851274-53851275	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs142441570	chr8:53851330-53851331	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs369986767	chr8:53851343-53851344	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs530676575	chr8:53851384-53851385	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs550755682	chr8:53851417-53851418	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545125	chr8:53851462-53851463	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs536437104	chr8:53851488-53851489	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545240	chr8:53851506-53851507	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs6997767	chr8:53851550-53851551	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562171061	chr8:53851581-53851582	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529320878	chr8:53851622-53851623	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs80353995	chr8:53851646-53851647	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs565898528	chr8:53851666-53851667	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs648531	chr8:53851670-53851671	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs186693742	chr8:53851684-53851685	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs558550184	chr8:53851777-53851778	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs372851814	chr8:53851780-53851781	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs376100924	chr8:53851808-53851809	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs192623748	chr8:53851869-53851870	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs555104210	chr8:53852037-53852038	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573684304	chr8:53852050-53852051	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534392986	chr8:53852159-53852160	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111543926	chr8:53852185-53852186	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552948998	chr8:53852186-53852187	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs41265256	chr8:53852204-53852205	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs546506426	chr8:53852209-53852210	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs41265258	chr8:53852231-53852232	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11994397	chr8:53852235-53852236	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs544032001	chr8:53852292-53852293	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140227793	chr8:53852311-53852312	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574969926	chr8:53852345-53852346	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529401248	chr8:53852403-53852404	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs145544643	chr8:53852405-53852406	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs560235944	chr8:53852416-53852417	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs147730838	chr8:53852426-53852427	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs367733073	chr8:53852441-53852442	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs533169358	chr8:53852462-53852463	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs551301677	chr8:53852472-53852473	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
2	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr8:53850600-53851200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
5	chr8:53850600-53851400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
6	chr8:53850800-53851200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
7	chr8:53850800-53853400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr8:53850800-53854400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
9	chr8:53851000-53851200	Bivalent Enhancer	Primary T cells from cord blood	blood
10	chr8:53851000-53851200	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
11	chr8:53851000-53851200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
12	chr8:53851000-53851400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
13	chr8:53851000-53851600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:53851000-53851800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
15	chr8:53851000-53851800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
16	chr8:53851000-53852000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr8:53851000-53852200	Bivalent Enhancer	Brain Anterior Caudate	brain
18	chr8:53851000-53852200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
19	chr8:53851000-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr8:53851000-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:53851000-53854600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
22	chr8:53851000-53854800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
23	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
24	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
25	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
26	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
27	chr8:53851200-53851400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
28	chr8:53851200-53851600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
29	chr8:53851200-53851600	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
30	chr8:53851200-53852600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
31	chr8:53851200-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
32	chr8:53851200-53854800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
33	chr8:53851200-53854800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
34	chr8:53851400-53851600	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
35	chr8:53851400-53851600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
36	chr8:53851400-53851800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr8:53851400-53851800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
38	chr8:53851400-53852000	Bivalent Enhancer	Primary B cells from cord blood	blood
39	chr8:53851400-53852000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
40	chr8:53851400-53852000	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
41	chr8:53851400-53852000	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr8:53851400-53852000	Bivalent Enhancer	Fetal Brain Male	brain
43	chr8:53851400-53852200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
44	chr8:53851400-53852200	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:53851400-53852200	Bivalent Enhancer	Liver	Liver
46	chr8:53851400-53852400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr8:53851400-53852600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
48	chr8:53851400-53852600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
49	chr8:53851400-53853000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:53851400-53853800	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood

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