Variant report

Variant	nsv429930
Chromosome Location	chr8:96317910-96454743
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:688)
CpG islands
(count:366)
Chromatin interactive
region (count:56)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:688 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:96371551-96371676	K562	blood:	n/a	n/a
2	ATF1	chr8:96391345-96391544	K562	blood:	n/a	n/a
3	ATF1	chr8:96398845-96399123	K562	blood:	n/a	n/a
4	ATF1	chr8:96329850-96330255	K562	blood:	n/a	n/a
5	ATF2	chr8:96374120-96375205	GM12878	blood:	n/a	n/a
6	ATF2	chr8:96374159-96375125	GM12878	blood:	n/a	n/a
7	BACH1	chr8:96420287-96420578	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr8:96388436-96389094	GM12878	blood:	n/a	n/a
9	BATF	chr8:96374687-96375007	GM12878	blood:	n/a	chr8:96374868-96374879
10	BATF	chr8:96374567-96375091	GM12878	blood:	n/a	chr8:96374868-96374879
11	BCL11A	chr8:96374629-96375037	GM12878	blood:	n/a	n/a
12	BCL3	chr8:96374554-96375247	GM12878	blood:	n/a	n/a
13	BCLAF1	chr8:96374174-96375215	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:96423422-96423554	K562	blood:	n/a	chr8:96423463-96423476 chr8:96423464-96423473 chr8:96423465-96423474 chr8:96423459-96423480 chr8:96423465-96423474 chr8:96423466-96423475
15	BHLHE40	chr8:96378565-96378611	K562	blood:	n/a	n/a
16	BHLHE40	chr8:96329767-96330097	K562	blood:	n/a	n/a
17	BHLHE40	chr8:96399044-96399107	K562	blood:	n/a	n/a
18	CCNT2	chr8:96329720-96329944	K562	blood:	n/a	n/a
19	CEBPB	chr8:96445313-96445477	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:96329718-96330115	K562	blood:	n/a	chr8:96329932-96329943 chr8:96329932-96329945 chr8:96329932-96329945
21	CEBPB	chr8:96325485-96325726	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr8:96346146-96346441	K562	blood:	n/a	n/a
23	CEBPB	chr8:96344776-96345042	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:96388347-96389008	GM12878	blood:	n/a	n/a
25	CEBPB	chr8:96449382-96449610	IMR90	lung:	n/a	chr8:96449516-96449527
26	CEBPB	chr8:96374131-96375280	GM12878	blood:	n/a	n/a
27	CEBPB	chr8:96344794-96344978	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:96324033-96324034	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:96449345-96449721	HepG2	liver:	n/a	chr8:96449516-96449527
30	CEBPB	chr8:96417560-96418117	IMR90	lung:	n/a	n/a
31	CEBPB	chr8:96329750-96330133	K562	blood:	n/a	chr8:96329932-96329943 chr8:96329932-96329945 chr8:96329932-96329945
32	CEBPB	chr8:96449408-96449593	A549	lung:	n/a	chr8:96449516-96449527
33	CEBPB	chr8:96346147-96346455	K562	blood:	n/a	n/a
34	CEBPD	chr8:96329687-96330082	K562	blood:	n/a	chr8:96329932-96329943
35	CEBPD	chr8:96391294-96391643	K562	blood:	n/a	n/a
36	CHD2	chr8:96420375-96420546	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr8:96377353-96377362	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTBP2	chr8:96442803-96443791	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr8:96398860-96399010	NHEK	skin:	n/a	n/a
40	CTCF	chr8:96317628-96317918	GM19240	blood:	n/a	chr8:96317782-96317800 chr8:96317784-96317805 chr8:96317783-96317799 chr8:96317785-96317798
41	CTCF	chr8:96398866-96399130	GM12878	blood:	n/a	n/a
42	CTCF	chr8:96378800-96378950	GM12873	blood:	n/a	n/a
43	CTCF	chr8:96398900-96399050	GM12875	blood:	n/a	n/a
44	CTCF	chr8:96398714-96399249	HCT-116	colon:	n/a	n/a
45	CTCF	chr8:96378780-96378930	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr8:96325520-96325670	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr8:96398940-96399090	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr8:96325600-96325750	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr8:96318040-96318190	HVMF	connective:	n/a	n/a
50	CTCF	chr8:96398940-96399090	GM12873	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:96377380-96377430	GM19239	blood:	n/a
2	chr8:96394047-96394097	HCF	heart:	n/a
3	chr8:96443153-96443203	AG04450	lung:	fetal
4	chr8:96418790-96418840	ProgFib	skin:	n/a
5	chr8:96387677-96387727	AG09319	gingival:	n/a
6	chr8:96393868-96393918	GM06990	blood:	n/a
7	chr8:96377380-96377430	NHDF-neo	bronchial:	n/a
8	chr8:96377380-96377430	GM12892	blood:	n/a
9	chr8:96393868-96393918	HCM	heart:	n/a
10	chr8:96377380-96377430	HAEpiC	amniotic membrane:	n/a
11	chr8:96443153-96443203	HL-60	blood:	n/a
12	chr8:96377380-96377430	AG10803	skin:	n/a
13	chr8:96443153-96443203	T-47D	breast:	n/a
14	chr8:96418790-96418840	NHDF-neo	bronchial:	n/a
15	chr8:96393868-96393918	HUVEC	blood vessel:	n/a
16	chr8:96387677-96387727	Hepatocyte	liver:	n/a
17	chr8:96393868-96393918	ECC-1	luminal epithelium:	n/a
18	chr8:96393868-96393918	SK-N-SH	brain:	n/a
19	chr8:96394047-96394097	AG09309	skin:	n/a
20	chr8:96387677-96387727	MCF10A-Er-Src	breast:	n/a
21	chr8:96387677-96387727	HEEpiC	esophagus:	n/a
22	chr8:96377380-96377430	HRCEpiC	kidney:	n/a
23	chr8:96377380-96377430	HIPEpiC	eye:	n/a
24	chr8:96387677-96387727	T-47D	breast:	n/a
25	chr8:96418790-96418840	PFSK-1	brain:	n/a
26	chr8:96418790-96418840	SK-N-SH_RA	brain:	n/a
27	chr8:96387677-96387727	HCPEpiC	choroid plexus:	n/a
28	chr8:96418790-96418840	HUVEC	blood vessel:	n/a
29	chr8:96394047-96394097	Caco-2	colon:	n/a
30	chr8:96418790-96418840	IMR90	lung:	fetal
31	chr8:96443153-96443203	SK-N-SH	brain:	n/a
32	chr8:96443153-96443203	Hepatocyte	liver:	n/a
33	chr8:96443153-96443203	RPTEC	kidney:	n/a
34	chr8:96394047-96394097	PFSK-1	brain:	n/a
35	chr8:96377380-96377430	H1-hESC	embryonic stem cell:	embryo
36	chr8:96393868-96393918	Hela-S3	cervix:	n/a
37	chr8:96418790-96418840	HCF	heart:	n/a
38	chr8:96387677-96387727	SKMC	muscle:	n/a
39	chr8:96387677-96387727	HRCEpiC	kidney:	n/a
40	chr8:96377380-96377430	BE2_C	brain:	n/a
41	chr8:96394047-96394097	SK-N-SH_RA	brain:	n/a
42	chr8:96377380-96377430	HMEC	breast:	n/a
43	chr8:96377380-96377430	A549	lung:	n/a
44	chr8:96387677-96387727	ECC-1	luminal epithelium:	n/a
45	chr8:96394047-96394097	BJ	skin:	n/a
46	chr8:96393868-96393918	SKMC	muscle:	n/a
47	chr8:96377380-96377430	SK-N-MC	brain:	n/a
48	chr8:96387677-96387727	HNPCEpiC	eye:	n/a
49	chr8:96377380-96377430	NT2-D1	testis:	n/a
50	chr8:96394047-96394097	AoSMC	blood vessel:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:96403419..96405368-chr8:96406859..96408584,2	MCF-7	breast:
2	chr8:96398409..96400158-chr8:96402287..96404999,2	K562	blood:
3	chr8:96347218..96348000-chr8:96398502..96399465,2	MCF-7	breast:
4	chr8:96394533..96397301-chr8:96397590..96400549,2	K562	blood:
5	chr8:96317249..96318240-chr8:96330378..96331048,2	MCF-7	breast:
6	chr8:96361749..96363597-chr8:96404852..96407172,2	MCF-7	breast:
7	chr8:96350551..96352730-chr8:96354541..96356363,2	K562	blood:
8	chr8:96350551..96352730-chr8:96354541..96356363,2	K562	blood:
9	chr8:96405823..96408644-chr8:96412280..96414202,2	K562	blood:
10	chr8:96317494..96318183-chr8:96770674..96771530,2	MCF-7	breast:
11	chr8:96350900..96352730-chr8:96354541..96356133,2	K562	blood:
12	chr8:96317394..96318355-chr8:96398480..96399433,5	MCF-7	breast:
13	chr8:96394533..96397301-chr8:96397590..96400549,2	K562	blood:
14	chr8:96316456..96319380-chr8:96320375..96323597,4	K562	blood:
15	chr8:96356776..96359648-chr8:96361298..96363539,2	K562	blood:
16	chr8:96317249..96318240-chr8:96330378..96331048,2	MCF-7	breast:
17	chr8:96316456..96319380-chr8:96319593..96323597,5	K562	blood:
18	chr8:96324375..96326603-chr8:96330016..96331695,2	MCF-7	breast:
19	chr8:96324375..96326603-chr8:96330016..96331695,2	MCF-7	breast:
20	chr8:96405059..96407686-chr8:96436292..96438669,2	K562	blood:
21	chr8:96370825..96374259-chr8:96378981..96380803,3	MCF-7	breast:
22	chr8:96361268..96364622-chr8:96368005..96369797,3	MCF-7	breast:
23	chr8:96361749..96363597-chr8:96404852..96407172,2	MCF-7	breast:
24	chr8:96361268..96364622-chr8:96368005..96369797,3	MCF-7	breast:
25	chr8:96410944..96413465-chr8:96415698..96417664,2	K562	blood:
26	chr8:96317509..96318201-chr8:97176319..97177107,2	MCF-7	breast:
27	chr8:96316456..96319380-chr8:96319593..96323597,5	K562	blood:
28	chr8:96430126..96432297-chr8:96457329..96459845,2	K562	blood:
29	chr8:96395483..96396047-chr8:96860958..96861815,2	MCF-7	breast:
30	chr8:96378611..96380607-chr8:96388094..96389903,3	MCF-7	breast:
31	chr8:96317358..96318200-chr8:96398470..96399351,2	MCF-7	breast:
32	chr8:96403419..96405368-chr8:96406859..96408584,2	MCF-7	breast:
33	chr8:96388697..96390727-chr8:96393564..96396229,2	K562	blood:
34	chr8:96280917..96283132-chr8:96317094..96319252,2	K562	blood:
35	chr8:96317136..96318202-chr8:96639831..96640470,3	MCF-7	breast:
36	chr8:96448397..96451100-chr8:96451208..96454533,3	MCF-7	breast:
37	chr8:96316456..96319380-chr8:96320375..96323597,4	K562	blood:
38	chr8:96333700..96336358-chr8:96336787..96340055,3	MCF-7	breast:
39	chr8:96096089..96098113-chr8:96363999..96366342,2	MCF-7	breast:
40	chr8:96333700..96336358-chr8:96336787..96340055,3	MCF-7	breast:
41	chr8:96378611..96380607-chr8:96388094..96389903,3	MCF-7	breast:
42	chr8:96356776..96359648-chr8:96361298..96363539,2	K562	blood:
43	chr8:96405823..96408644-chr8:96412280..96414202,2	K562	blood:
44	chr8:96398409..96400158-chr8:96402287..96404999,2	K562	blood:
45	chr8:96398658..96400358-chr8:96400929..96403787,2	K562	blood:
46	chr8:96317456..96318284-chr8:96770359..96771524,5	MCF-7	breast:
47	chr8:96317394..96318355-chr8:96398480..96399433,5	MCF-7	breast:
48	chr8:96448397..96451100-chr8:96451208..96454533,3	MCF-7	breast:
49	chr8:96317358..96318200-chr8:96398470..96399351,2	MCF-7	breast:
50	chr8:96388697..96390727-chr8:96393564..96396229,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHF2-2	chr8:96444854-96445008	NONHSAT127835
2	lnc-PLEKHF2-2	chr8:96444854-96444894	ENSG00000253773.1
3	lnc-PLEKHF2-2	chr8:96444854-96445008	NONHSAT127831
4	lnc-PLEKHF2-2	chr8:96356511-96356673	NONHSAT127829
5	lnc-PLEKHF2-2	chr8:96444854-96445008	NONHSAT127837
6	lnc-PLEKHF2-2	chr8:96444854-96445008	ENSG00000253773.1
7	lnc-PLEKHF2-2	chr8:96444865-96445008	ENSG00000253773.1

No data

Variant related genes	Relation type
ENSG00000253773	TF binding region
ENSG00000253945	TF binding region
ENSG00000253773	CpG island
ENSG00000253945	CpG island
ENSG00000253773	chromatin interactions
ENSG00000253945	chromatin interactions
ENSG00000156172	chromatin interactions

Extended variants
information (count: 3266 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:3266 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1994794	chr8:96317910-96317911	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76128055	chr8:96317920-96317921	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs111289145	chr8:96317937-96317938	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs527643509	chr8:96318031-96318032	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs547781131	chr8:96318063-96318064	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs369823006	chr8:96318064-96318065	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs374897612	chr8:96318067-96318068	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs550786155	chr8:96318082-96318083	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs538849664	chr8:96318125-96318126	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs530193626	chr8:96318126-96318127	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs550330235	chr8:96318127-96318128	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs569061584	chr8:96318132-96318133	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs62524431	chr8:96318206-96318207	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557719382	chr8:96318217-96318218	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs571527430	chr8:96318282-96318283	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs533519170	chr8:96318288-96318289	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs377539891	chr8:96318305-96318306	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs565853869	chr8:96318315-96318316	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553751579	chr8:96318325-96318326	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543794554	chr8:96318330-96318331	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs557202452	chr8:96318349-96318350	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs74912335	chr8:96318428-96318429	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142094022	chr8:96318441-96318442	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs545589561	chr8:96318458-96318459	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs574492675	chr8:96318472-96318473	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs565402328	chr8:96318522-96318523	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs151200127	chr8:96318571-96318572	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs541040337	chr8:96318574-96318575	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs74928366	chr8:96318605-96318606	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs398086819	chr8:96318606-96318607	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs398073344	chr8:96318607-96318608	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs561248708	chr8:96318656-96318657	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs190264619	chr8:96318677-96318678	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs369031990	chr8:96318837-96318838	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs182507953	chr8:96318935-96318936	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs557442033	chr8:96318936-96318937	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs550943620	chr8:96318942-96318943	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577237294	chr8:96318959-96318960	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs139133229	chr8:96318979-96318980	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs546256694	chr8:96319002-96319003	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs55755604	chr8:96319006-96319007	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs149964950	chr8:96319023-96319024	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs571421772	chr8:96319035-96319036	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs187967387	chr8:96319092-96319093	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs77502294	chr8:96319115-96319116	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs398095976	chr8:96319123-96319124	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs375709685	chr8:96319207-96319208	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs375836335	chr8:96319312-96319313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547323788	chr8:96319318-96319319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566913221	chr8:96319396-96319397	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96317400-96318000	Enhancers	Brain Inferior Temporal Lobe	brain
2	chr8:96317400-96318200	Bivalent Enhancer	Osteobl	bone
3	chr8:96317800-96318400	Enhancers	Colon Smooth Muscle	Colon
4	chr8:96318800-96319200	Enhancers	Colon Smooth Muscle	Colon
5	chr8:96318800-96319600	Enhancers	Rectal Smooth Muscle	rectum
6	chr8:96319200-96319400	Enhancers	Brain Germinal Matrix	brain
7	chr8:96324800-96325000	Enhancers	Brain Hippocampus Middle	brain
8	chr8:96326400-96327400	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr8:96326800-96327000	Enhancers	Brain Germinal Matrix	brain
10	chr8:96326800-96328200	Enhancers	Brain Anterior Caudate	brain
11	chr8:96327000-96327600	Weak transcription	Brain Germinal Matrix	brain
12	chr8:96327000-96328000	Enhancers	Brain Angular Gyrus	brain
13	chr8:96327000-96328200	Enhancers	Pancreas	Pancrea
14	chr8:96327000-96329800	Enhancers	Brain Substantia Nigra	brain
15	chr8:96327200-96330200	Enhancers	Brain Hippocampus Middle	brain
16	chr8:96327400-96327600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
17	chr8:96327400-96330200	Enhancers	Brain Cingulate Gyrus	brain
18	chr8:96327600-96328000	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr8:96327600-96328200	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr8:96327600-96329000	Enhancers	Brain Germinal Matrix	brain
21	chr8:96328000-96328800	Weak transcription	Brain Angular Gyrus	brain
22	chr8:96328200-96329400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr8:96328200-96330600	Weak transcription	Pancreas	Pancrea
24	chr8:96328800-96330000	Enhancers	Brain Angular Gyrus	brain
25	chr8:96329000-96330600	Enhancers	Stomach Mucosa	stomach
26	chr8:96329000-96330800	Enhancers	Fetal Intestine Large	intestine
27	chr8:96329200-96330600	Enhancers	Fetal Intestine Small	intestine
28	chr8:96329400-96330000	Enhancers	Fetal Heart	heart
29	chr8:96329400-96330200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr8:96329400-96330200	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr8:96329400-96330800	Enhancers	Duodenum Mucosa	Duodenum
32	chr8:96329400-96331600	Enhancers	Liver	Liver
33	chr8:96329600-96330000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:96329800-96330000	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr8:96329800-96330400	Enhancers	HUVEC	blood vessel
36	chr8:96329800-96330400	Enhancers	K562	blood
37	chr8:96329800-96330800	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr8:96329800-96330800	Enhancers	Right Atrium	heart
39	chr8:96330600-96330800	Enhancers	Lung	lung
40	chr8:96330600-96331200	Enhancers	Pancreas	Pancrea
41	chr8:96344400-96344600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:96345600-96346200	Enhancers	Fetal Intestine Large	intestine
43	chr8:96345600-96348000	Enhancers	Fetal Intestine Small	intestine
44	chr8:96346200-96346600	Weak transcription	Fetal Intestine Large	intestine
45	chr8:96346600-96348000	Enhancers	Fetal Intestine Large	intestine
46	chr8:96346800-96347000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:96347000-96353200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:96348200-96348600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr8:96348200-96349000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:96348600-96349000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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