Variant report

Variant	nsv534270
Chromosome Location	chr8:113585830-113979075
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	ATF1	chr8:113711892-113712099	K562	blood:	n/a	n/a
2	BACH1	chr8:113922706-113922831	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:113894395-113894840	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:113896385-113896632	GM12878	blood:	n/a	n/a
5	BCL3	chr8:113882242-113882516	GM12878	blood:	n/a	n/a
6	BCL3	chr8:113623801-113624046	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:113927174-113927201	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:113908499-113908568	K562	blood:	n/a	n/a
9	BHLHE40	chr8:113896504-113896523	GM12878	blood:	n/a	n/a
10	CEBPB	chr8:113944306-113944556	A549	lung:	n/a	n/a
11	CEBPB	chr8:113974921-113975698	Hela-S3	cervix:	n/a	chr8:113975575-113975586 chr8:113975593-113975606
12	CEBPB	chr8:113821058-113821309	HepG2	liver:	n/a	chr8:113821154-113821165 chr8:113821155-113821166 chr8:113821207-113821220 chr8:113821154-113821165 chr8:113821207-113821218 chr8:113821207-113821218 chr8:113821154-113821167 chr8:113821208-113821219
13	CEBPB	chr8:113680956-113681228	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:113675826-113676181	IMR90	lung:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
15	CEBPB	chr8:113745665-113745746	H1-hESC	embryonic stem cell:	n/a	chr8:113745713-113745726 chr8:113745713-113745726
16	CEBPB	chr8:113675862-113676155	H1-hESC	embryonic stem cell:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
17	CEBPB	chr8:113754057-113754327	HepG2	liver:	n/a	chr8:113754141-113754152 chr8:113754140-113754153
18	CEBPB	chr8:113675869-113676172	K562	blood:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
19	CEBPB	chr8:113950231-113950545	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr8:113906390-113906592	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr8:113841913-113842215	HepG2	liver:	n/a	chr8:113842057-113842066 chr8:113842055-113842068 chr8:113842056-113842067
22	CEBPB	chr8:113792268-113792556	HepG2	liver:	n/a	chr8:113792436-113792447
23	CEBPB	chr8:113844073-113844272	HepG2	liver:	n/a	chr8:113844206-113844217
24	CEBPB	chr8:113628682-113629030	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:113675839-113676180	Hela-S3	cervix:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
26	CEBPB	chr8:113811038-113811324	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:113808330-113808550	HepG2	liver:	n/a	chr8:113808414-113808427 chr8:113808414-113808425 chr8:113808414-113808427
28	CEBPB	chr8:113675839-113676178	MCF-7	breast:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
29	CEBPB	chr8:113675853-113676190	A549	lung:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
30	CEBPB	chr8:113705928-113706157	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:113973274-113973549	HepG2	liver:	n/a	chr8:113973303-113973314 chr8:113973425-113973436 chr8:113973303-113973312
32	CEBPB	chr8:113976943-113977580	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:113675831-113676188	HepG2	liver:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
34	CEBPB	chr8:113682533-113683041	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr8:113946021-113946417	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr8:113695353-113695608	HepG2	liver:	n/a	n/a
37	CHD2	chr8:113785202-113785205	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr8:113774260-113774410	NHEK	skin:	n/a	chr8:113774322-113774332 chr8:113774317-113774335 chr8:113774319-113774340 chr8:113774318-113774334
39	CTCF	chr8:113774220-113774370	GM12872	blood:	n/a	chr8:113774322-113774332 chr8:113774317-113774335 chr8:113774319-113774340 chr8:113774318-113774334
40	CTCF	chr8:113819120-113819270	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr8:113774200-113774350	BJ	skin:	n/a	chr8:113774322-113774332 chr8:113774317-113774335 chr8:113774319-113774340 chr8:113774318-113774334
42	CTCF	chr8:113813421-113813632	Gliobla	brain:	n/a	chr8:113813509-113813522 chr8:113813508-113813529 chr8:113813506-113813524 chr8:113813507-113813523
43	CTCF	chr8:113813420-113813570	GM12874	blood:	n/a	chr8:113813509-113813522 chr8:113813508-113813529 chr8:113813506-113813524 chr8:113813507-113813523
44	CTCF	chr8:113774220-113774370	GM12867	blood:	n/a	chr8:113774322-113774332 chr8:113774317-113774335 chr8:113774319-113774340 chr8:113774318-113774334
45	CTCF	chr8:113774280-113774430	HFF-Myc	foreskin:	n/a	chr8:113774322-113774332 chr8:113774317-113774335 chr8:113774319-113774340 chr8:113774318-113774334
46	CTCF	chr8:113813460-113813610	HCM	heart:	n/a	chr8:113813509-113813522 chr8:113813508-113813529 chr8:113813506-113813524 chr8:113813507-113813523
47	CTCF	chr8:113813400-113813550	AoAF	blood vessel:	n/a	chr8:113813509-113813522 chr8:113813508-113813529 chr8:113813506-113813524 chr8:113813507-113813523
48	CTCF	chr8:113774240-113774390	GM06990	blood:	n/a	chr8:113774322-113774332 chr8:113774317-113774335 chr8:113774319-113774340 chr8:113774318-113774334
49	CTCF	chr8:113813420-113813570	AG09319	gingival:	n/a	chr8:113813509-113813522 chr8:113813508-113813529 chr8:113813506-113813524 chr8:113813507-113813523
50	CTCF	chr8:113774166-113774471	K562	blood:	n/a	chr8:113774322-113774332 chr8:113774317-113774335 chr8:113774319-113774340 chr8:113774318-113774334

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:113818694-113818744	Hela-S3	cervix:	n/a
2	chr8:113818694-113818744	ECC-1	luminal epithelium:	n/a
3	chr8:113656015-113656065	HUVEC	blood vessel:	n/a
4	chr8:113703176-113703226	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:113818694-113818744	HEEpiC	esophagus:	n/a
6	chr8:113818694-113818744	NHBE	bronchial:	n/a
7	chr8:113655436-113655486	NB4	blood:	n/a
8	chr8:113655436-113655486	AG10803	skin:	n/a
9	chr8:113703176-113703226	HNPCEpiC	eye:	n/a
10	chr8:113702707-113702757	SK-N-MC	brain:	n/a
11	chr8:113655561-113655611	NH-A	brain:	n/a
12	chr8:113655561-113655611	SKMC	muscle:	n/a
13	chr8:113703176-113703226	ProgFib	skin:	n/a
14	chr8:113702707-113702757	NH-A	brain:	n/a
15	chr8:113703176-113703226	IMR90	lung:	fetal
16	chr8:113655436-113655486	HPAEpiC	pulmonary alveolar:	n/a
17	chr8:113703176-113703226	HCM	heart:	n/a
18	chr8:113703176-113703226	A549	lung:	n/a
19	chr8:113655561-113655611	SK-N-MC	brain:	n/a
20	chr8:113656015-113656065	HAEpiC	amniotic membrane:	n/a
21	chr8:113655561-113655611	Hepatocyte	liver:	n/a
22	chr8:113655561-113655611	LNCaP	prostate:	n/a
23	chr8:113655561-113655611	HL-60	blood:	n/a
24	chr8:113655561-113655611	A549	lung:	n/a
25	chr8:113656015-113656065	PFSK-1	brain:	n/a
26	chr8:113655561-113655611	GM06990	blood:	n/a
27	chr8:113655436-113655486	U87	brain:	n/a
28	chr8:113702707-113702757	HRE	kidney:	n/a
29	chr8:113702707-113702757	A549	lung:	n/a
30	chr8:113702707-113702757	AG10803	skin:	n/a
31	chr8:113656015-113656065	Caco-2	colon:	n/a
32	chr8:113818694-113818744	AG09319	gingival:	n/a
33	chr8:113655436-113655486	SAEC	small airway:	n/a
34	chr8:113703176-113703226	MCF-7	breast:	n/a
35	chr8:113703176-113703226	SK-N-SH	brain:	n/a
36	chr8:113655436-113655486	HAEpiC	amniotic membrane:	n/a
37	chr8:113656015-113656065	ovcar-3	ovarian:	n/a
38	chr8:113703176-113703226	PrEC	prostate:	n/a
39	chr8:113656015-113656065	PANC-1	pancreas:	n/a
40	chr8:113656015-113656065	H1-hESC	embryonic stem cell:	embryo
41	chr8:113655561-113655611	HCM	heart:	n/a
42	chr8:113655436-113655486	Jurkat	blood:	n/a
43	chr8:113655436-113655486	BE2_C	brain:	n/a
44	chr8:113655561-113655611	HAEpiC	amniotic membrane:	n/a
45	chr8:113656015-113656065	BE2_C	brain:	n/a
46	chr8:113655561-113655611	PrEC	prostate:	n/a
47	chr8:113656015-113656065	HMEC	breast:	n/a
48	chr8:113655436-113655486	GM19239	blood:	n/a
49	chr8:113818694-113818744	PANC-1	pancreas:	n/a
50	chr8:113818694-113818744	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:113623376..113625406-chr8:113626015..113627569,2	MCF-7	breast:
2	chr8:113719443..113721302-chr8:113723054..113725365,2	K562	blood:
3	chr8:113812991..113814473-chr8:114449636..114450437,5	MCF-7	breast:
4	chr8:112878252..112879995-chr8:113601916..113604196,2	MCF-7	breast:
5	chr8:113656932..113658484-chr8:113659367..113661819,2	K562	blood:
6	chr8:113773910..113774788-chr8:114210759..114211408,2	MCF-7	breast:
7	chr8:113813041..113814009-chr8:114183692..114184450,5	MCF-7	breast:
8	chr8:113719443..113721302-chr8:113723054..113725365,2	K562	blood:
9	chr3:185653287..185655288-chr8:113877614..113879705,2	MCF-7	breast:
10	chr8:113648317..113650428-chr8:113651221..113653011,2	MCF-7	breast:
11	chr8:113882423..113884756-chr8:114016772..114018870,2	K562	blood:
12	chr8:113753759..113755315-chr8:113758540..113760790,2	MCF-7	breast:
13	chr8:113773909..113774597-chr8:114183855..114184506,4	MCF-7	breast:
14	chr8:113623376..113625406-chr8:113626015..113627569,2	MCF-7	breast:
15	chr8:113730328..113732083-chr8:113748434..113750301,2	K562	blood:
16	chr8:113730328..113732083-chr8:113748434..113750301,2	K562	blood:
17	chr8:113812932..113813631-chr8:114183972..114184626,2	MCF-7	breast:
18	chr8:113774045..113774707-chr8:114449888..114450422,3	MCF-7	breast:
19	chr20:18661388..18664062-chr8:113586254..113588798,2	MCF-7	breast:
20	chr11:85195583..85198227-chr8:113682885..113684772,2	MCF-7	breast:
21	chr8:113753759..113755315-chr8:113758540..113760790,2	MCF-7	breast:
22	chr8:113774348..113777140-chr8:114064225..114066718,2	K562	blood:
23	chr8:113659187..113660730-chr8:113666931..113668583,2	MCF-7	breast:
24	chr8:113948637..113951504-chr8:113954981..113956955,2	K562	blood:
25	chr8:113774024..113774627-chr8:114390471..114391174,2	MCF-7	breast:
26	chr8:113656932..113658484-chr8:113659367..113661819,2	K562	blood:
27	chr6:30778063..30780102-chr8:113652986..113654698,2	MCF-7	breast:
28	chr8:113659187..113660730-chr8:113666931..113668583,2	MCF-7	breast:
29	chr8:113948637..113951504-chr8:113954981..113956955,2	K562	blood:
30	chr8:113648317..113650428-chr8:113651221..113653011,2	MCF-7	breast:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-2053	chr8:113655782-113655804	MIMAT0009978

Variant related genes	Relation type
CSMD3	TF binding region
MIR2053	TF binding region
CSMD3	CpG island
MIR2053	CpG island
ENSG00000136527	chromatin interactions

Extended variants
information (count: 8319 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:8319 , 50 per page) page: 1 2 3 4 5 6 7 ... 167

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562559087	chr8:113585853-113585854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143652338	chr8:113585861-113585862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200793759	chr8:113585863-113585864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141834837	chr8:113585874-113585875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199762300	chr8:113585882-113585883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374591869	chr8:113585890-113585891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372024428	chr8:113585903-113585904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374220485	chr8:113585933-113585934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539932134	chr8:113585945-113585946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190896883	chr8:113585953-113585954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528657328	chr8:113585971-113585972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551985778	chr8:113585976-113585977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565408458	chr8:113586032-113586033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531256188	chr8:113586077-113586078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111707810	chr8:113586089-113586090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs180832069	chr8:113586110-113586111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186513919	chr8:113586114-113586115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34774124	chr8:113586152-113586153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545026686	chr8:113586155-113586156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546754966	chr8:113586162-113586163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs6981829	chr8:113586164-113586165	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs538419454	chr8:113586166-113586167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374471737	chr8:113586179-113586180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370751610	chr8:113586197-113586198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150388610	chr8:113586202-113586203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568764088	chr8:113586222-113586223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11776962	chr8:113586228-113586229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs368803982	chr8:113586247-113586248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11783840	chr8:113586276-113586277	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs574092236	chr8:113586277-113586278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76623397	chr8:113586283-113586284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553571656	chr8:113586363-113586364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576888134	chr8:113586364-113586365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545245771	chr8:113586382-113586383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146969861	chr8:113586404-113586405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1453091	chr8:113586458-113586459	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs374183942	chr8:113586514-113586515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191419365	chr8:113586598-113586599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544913150	chr8:113586673-113586674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112500204	chr8:113586691-113586692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2853249	chr8:113586789-113586790	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs546985538	chr8:113586810-113586811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566821242	chr8:113586829-113586830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532642099	chr8:113586859-113586860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552044734	chr8:113586880-113586881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187418283	chr8:113586891-113586892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542987562	chr8:113586926-113586927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376851026	chr8:113586978-113586979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138088401	chr8:113586998-113586999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10102321	chr8:113587019-113587020	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	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
Glioblastoma multiforme	21080181	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Schizophrenia	20967226	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113555600-113594000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:113590600-113591200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr8:113590600-113591200	Enhancers	Brain Cingulate Gyrus	brain
4	chr8:113591200-113592800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr8:113592000-113592800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:113592200-113592600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr8:113592400-113593000	Enhancers	Brain Hippocampus Middle	brain
8	chr8:113592400-113593200	Enhancers	Brain Substantia Nigra	brain
9	chr8:113592600-113593000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr8:113592600-113593000	Enhancers	Brain Anterior Caudate	brain
11	chr8:113592800-113593200	Enhancers	Brain Angular Gyrus	brain
12	chr8:113593000-113593200	Enhancers	Brain Cingulate Gyrus	brain
13	chr8:113594000-113594600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:113594600-113623800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:113614800-113619800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:113621600-113623200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr8:113623200-113627600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:113623800-113624800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:113624800-113628800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:113627600-113630000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr8:113628000-113629400	Enhancers	HMEC	breast
22	chr8:113628200-113629400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:113628600-113629200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr8:113628600-113629200	Enhancers	Hela-S3	cervix
25	chr8:113628600-113629200	Enhancers	NHEK	skin
26	chr8:113628800-113629200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr8:113628800-113629200	Enhancers	NH-A	brain
28	chr8:113628800-113629400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:113629200-113680600	Weak transcription	NHEK	skin
30	chr8:113629400-113629800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:113629400-113661800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr8:113629800-113630200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr8:113633800-113634200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr8:113636200-113663600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr8:113636800-113680400	Weak transcription	HMEC	breast
36	chr8:113639600-113640000	Enhancers	Fetal Lung	lung
37	chr8:113640000-113644200	Weak transcription	Fetal Lung	lung
38	chr8:113644200-113644800	Enhancers	Fetal Lung	lung
39	chr8:113644200-113645800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:113645800-113649000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr8:113649000-113651200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:113655600-113656000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr8:113661800-113663400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:113663400-113676600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr8:113663600-113664400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr8:113664400-113666000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:113666000-113666400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:113666400-113675800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:113673600-113674000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr8:113675800-113678400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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