Variant report

Variant	esv34065
Chromosome Location	chr8:5824905-6143052
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	chr8:6061487-6061529	K562	blood:	n/a	n/a
2	BACH1	chr8:5997567-5997673	K562	blood:	n/a	n/a
3	BACH1	chr8:5850953-5851324	K562	blood:	n/a	n/a
4	BATF	chr8:6125905-6126127	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:5851125-5851150	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:5851096-5851152	K562	blood:	n/a	n/a
7	BHLHE40	chr8:5997564-5997834	K562	blood:	n/a	n/a
8	BHLHE40	chr8:5833612-5833750	GM12878	blood:	n/a	n/a
9	BRCA1	chr8:5848023-5848042	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr8:5934620-5934703	GM12878	blood:	n/a	n/a
11	BRCA1	chr8:5875790-5876111	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr8:5934404-5934557	HepG2	liver:	n/a	n/a
13	BRCA1	chr8:5850952-5851325	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr8:5978204-5978460	HepG2	liver:	n/a	chr8:5978303-5978315 chr8:5978298-5978309
15	CEBPB	chr8:5923564-5923858	IMR90	lung:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
16	CEBPB	chr8:5875401-5876188	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr8:6037962-6038464	A549	lung:	n/a	chr8:6038076-6038087 chr8:6038225-6038236 chr8:6038076-6038089 chr8:6038076-6038089 chr8:6038076-6038087
18	CEBPB	chr8:5992286-5992654	HepG2	liver:	n/a	chr8:5992465-5992478 chr8:5992465-5992476
19	CEBPB	chr8:6106947-6107139	MCF-7	breast:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
20	CEBPB	chr8:5992332-5992648	A549	lung:	n/a	chr8:5992465-5992478 chr8:5992465-5992476
21	CEBPB	chr8:5923557-5923830	HepG2	liver:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
22	CEBPB	chr8:6066396-6066631	A549	lung:	n/a	chr8:6066452-6066463 chr8:6066451-6066464 chr8:6066451-6066464 chr8:6066451-6066462
23	CEBPB	chr8:6038148-6038455	A549	lung:	n/a	chr8:6038225-6038236
24	CEBPB	chr8:5920888-5921158	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:6083799-6084067	HepG2	liver:	n/a	chr8:6083939-6083950
26	CEBPB	chr8:6038057-6038393	IMR90	lung:	n/a	chr8:6038076-6038087 chr8:6038225-6038236 chr8:6038076-6038089 chr8:6038076-6038089 chr8:6038076-6038087
27	CEBPB	chr8:5930436-5930514	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:5943713-5943758	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:5871254-5871589	IMR90	lung:	n/a	chr8:5871421-5871434
30	CEBPB	chr8:6100276-6100536	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:5903426-5903622	A549	lung:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
32	CEBPB	chr8:6128333-6128520	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr8:5903392-5903683	K562	blood:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
34	CEBPB	chr8:5917232-5917357	HepG2	liver:	n/a	chr8:5917295-5917306
35	CEBPB	chr8:6026345-6026672	IMR90	lung:	n/a	chr8:6026509-6026520 chr8:6026351-6026363
36	CEBPB	chr8:5923536-5923736	K562	blood:	n/a	chr8:5923710-5923721 chr8:5923708-5923719
37	CEBPB	chr8:6026433-6026617	H1-hESC	embryonic stem cell:	n/a	chr8:6026509-6026520
38	CEBPB	chr8:6037933-6038425	Hela-S3	cervix:	n/a	chr8:6038076-6038087 chr8:6038225-6038236 chr8:6038076-6038089 chr8:6038076-6038089 chr8:6038076-6038087
39	CEBPB	chr8:6100264-6100476	A549	lung:	n/a	n/a
40	CEBPB	chr8:6026359-6026690	HepG2	liver:	n/a	chr8:6026509-6026520
41	CEBPB	chr8:5850953-5851324	K562	blood:	n/a	n/a
42	CEBPB	chr8:5871279-5871583	K562	blood:	n/a	chr8:5871421-5871434
43	CEBPB	chr8:6066362-6066643	HepG2	liver:	n/a	chr8:6066452-6066463 chr8:6066451-6066464 chr8:6066451-6066464 chr8:6066451-6066462
44	CEBPB	chr8:5931821-5932072	K562	blood:	n/a	n/a
45	CEBPB	chr8:5903414-5903669	HepG2	liver:	n/a	chr8:5903521-5903534 chr8:5903518-5903535 chr8:5903521-5903532
46	CEBPB	chr8:5855136-5855336	HepG2	liver:	n/a	chr8:5855245-5855256
47	CEBPB	chr8:6083848-6084042	A549	lung:	n/a	chr8:6083939-6083950
48	CEBPB	chr8:6026333-6026694	A549	lung:	n/a	chr8:6026509-6026520 chr8:6026351-6026363
49	CEBPB	chr8:5850585-5850618	HepG2	liver:	n/a	chr8:5850591-5850602
50	CEBPB	chr8:6106856-6107207	HepG2	liver:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5910061-5910111	NH-A	brain:	n/a
2	chr8:5910061-5910111	NH-A	brain:	n/a
3	chr8:5909945-5909995	GM06990	blood:	n/a
4	chr8:5910061-5910111	AoSMC	blood vessel:	n/a
5	chr8:5910061-5910111	MCF-7	breast:	n/a
6	chr8:5992822-5992872	HEEpiC	esophagus:	n/a
7	chr8:6118575-6118625	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:5909880-5909930	HL-60	blood:	n/a
9	chr8:5949290-5949340	HEK293	kidney:	embryo
10	chr8:5909945-5909995	H1-hESC	embryonic stem cell:	embryo
11	chr8:6118575-6118625	HL-60	blood:	n/a
12	chr8:6010288-6010338	HNPCEpiC	eye:	n/a
13	chr8:5902873-5902923	Hela-S3	cervix:	n/a
14	chr8:5909880-5909930	Caco-2	colon:	n/a
15	chr8:6118526-6118576	AoSMC	blood vessel:	n/a
16	chr8:5909945-5909995	GM19239	blood:	n/a
17	chr8:6118526-6118576	Hepatocyte	liver:	n/a
18	chr8:6118575-6118625	T-47D	breast:	n/a
19	chr8:5909880-5909930	BE2_C	brain:	n/a
20	chr8:6118575-6118625	GM19239	blood:	n/a
21	chr8:6010288-6010338	AG04449	skin:	fetal
22	chr8:5992822-5992872	GM12878	blood:	n/a
23	chr8:5992822-5992872	NHDF-neo	bronchial:	n/a
24	chr8:5910061-5910111	GM12891	blood:	n/a
25	chr8:5909945-5909995	SKMC	muscle:	n/a
26	chr8:5909880-5909930	RPTEC	kidney:	n/a
27	chr8:5902873-5902923	BJ	skin:	n/a
28	chr8:6118575-6118625	Hela-S3	cervix:	n/a
29	chr8:6010199-6010249	SK-N-SH_RA	brain:	n/a
30	chr8:6010199-6010249	PFSK-1	brain:	n/a
31	chr8:5992822-5992872	HepG2	liver:	n/a
32	chr8:5910061-5910111	GM12892	blood:	n/a
33	chr8:6010199-6010249	AG09319	gingival:	n/a
34	chr8:6010288-6010338	T-47D	breast:	n/a
35	chr8:6118526-6118576	NB4	blood:	n/a
36	chr8:5902873-5902923	AG10803	skin:	n/a
37	chr8:6118526-6118576	BJ	skin:	n/a
38	chr8:5949290-5949340	AG04449	skin:	fetal
39	chr8:5910061-5910111	SKMC	muscle:	n/a
40	chr8:5992822-5992872	BJ	skin:	n/a
41	chr8:5910061-5910111	HIPEpiC	eye:	n/a
42	chr8:5902873-5902923	PrEC	prostate:	n/a
43	chr8:5949290-5949340	CMK	blood:	n/a
44	chr8:5909880-5909930	HAEpiC	amniotic membrane:	n/a
45	chr8:5992822-5992872	Hepatocyte	liver:	n/a
46	chr8:5992822-5992872	SK-N-MC	brain:	n/a
47	chr8:5992822-5992872	HMEC	breast:	n/a
48	chr8:6118575-6118625	ECC-1	luminal epithelium:	n/a
49	chr8:5910061-5910111	AG04449	skin:	fetal
50	chr8:5902873-5902923	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:6115787..6116559-chr8:6229328..6229869,2	MCF-7	breast:
2	chr8:6084910..6087836-chr8:6095267..6098254,2	K562	blood:
3	chr8:5917249..5917976-chr8:5997130..5997653,2	MCF-7	breast:
4	chr8:5933019..5935981-chr8:5937353..5939270,2	K562	blood:
5	chr8:5905980..5908043-chr8:5909546..5912210,2	K562	blood:
6	chr8:4919838..4920394-chr8:5997449..5998189,2	K562	blood:
7	chr8:5543604..5544126-chr8:5997197..5997756,2	MCF-7	breast:
8	chr8:5990205..5992800-chr8:5992973..5994775,2	K562	blood:
9	chr8:5990205..5992800-chr8:5992973..5994775,2	K562	blood:
10	chr8:6116111..6116635-chr8:6188825..6189362,2	MCF-7	breast:
11	chr8:6040393..6043249-chr8:6044843..6046899,2	K562	blood:
12	chr8:6079332..6082540-chr8:6084426..6086508,3	K562	blood:
13	chr8:6080157..6081666-chr8:6091415..6093477,2	MCF-7	breast:
14	chr8:6080157..6081666-chr8:6091415..6093477,2	MCF-7	breast:
15	chr8:4919533..4920406-chr8:5997153..5998101,2	MCF-7	breast:
16	chr8:5933019..5935981-chr8:5937353..5939270,2	K562	blood:
17	chr8:5933019..5936001-chr8:5936013..5938853,2	K562	blood:
18	chr10:132324298..132325038-chr8:6023084..6023812,2	MCF-7	breast:
19	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
20	chr8:6079332..6082540-chr8:6084426..6086508,3	K562	blood:
21	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
22	chr8:5917249..5917976-chr8:5997130..5997653,2	MCF-7	breast:
23	chr8:6106618..6108795-chr8:6113891..6116770,2	K562	blood:
24	chr8:5797855..5798416-chr8:5934095..5934883,2	MCF-7	breast:
25	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
26	chr8:6040393..6043249-chr8:6044843..6046899,2	K562	blood:
27	chr8:5933019..5936001-chr8:5936013..5938853,2	K562	blood:
28	chr8:5905980..5908043-chr8:5909546..5912210,2	K562	blood:
29	chr8:6084910..6087836-chr8:6095267..6098254,2	K562	blood:
30	chr8:6115678..6116241-chr8:6687345..6688278,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-3	chr8:5917266-5917339	ENSG00000253880
2	lnc-ANGPT2-3	chr8:5923520-5923650	XLOC_006984
3	lnc-ANGPT2-4	chr8:5893955-5893990	ENSG00000253189
4	lnc-ANGPT2-3	chr8:5957850-5957973	ENSG00000253880
5	lnc-ANGPT2-4	chr8:5894123-5894292	ENSG00000253189
6	lnc-ANGPT2-3	chr8:5901875-5902047	ENSG00000253880
7	lnc-ANGPT2-5	chr8:5858959-5859084	XLOC_006983
8	lnc-ANGPT2-3	chr8:5916281-5916302	XLOC_006984
9	lnc-ANGPT2-3	chr8:6114933-6115058	ENSG00000253880
10	lnc-ANGPT2-3	chr8:5916524-5916600	ENSG00000253880
11	lnc-ANGPT2-3	chr8:5916524-5916659	XLOC_006984
12	lnc-ANGPT2-4	chr8:5894372-5894496	ENSG00000253189
13	lnc-ANGPT2-3	chr8:5917266-5917339	XLOC_006984
14	lnc-ANGPT2-5	chr8:5860524-5860623	XLOC_006983
15	lnc-ANGPT2-11	chr8:6082847-6083064	NONHSAT124769

Variant related genes	Relation type
ENSG00000253880	TF binding region
ENSG00000253189	TF binding region
ENSG00000253880	CpG island
ENSG00000253189	CpG island
ENSG00000253880	chromatin interactions
ACVR1B	miRNA target sites
ACVR2A	miRNA target sites

Extended variants
information (count: 12288 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:12288 , 50 per page) page: 1 2 3 4 5 6 7 ... 246

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13259125	chr8:5824905-5824906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562560147	chr8:5824982-5824983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs36121805	chr8:5824983-5824984	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs56412013	chr8:5824989-5824990	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs76943548	chr8:5824990-5824991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558394575	chr8:5825001-5825002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115489935	chr8:5825013-5825014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534127787	chr8:5825021-5825022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371595097	chr8:5825033-5825034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144053625	chr8:5825040-5825041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555875565	chr8:5825042-5825043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10105067	chr8:5825065-5825066	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541429670	chr8:5825092-5825093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556567949	chr8:5825095-5825096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577871232	chr8:5825104-5825105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182501255	chr8:5825106-5825107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576632944	chr8:5825116-5825117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544861667	chr8:5825118-5825119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185901021	chr8:5825121-5825122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147249191	chr8:5825123-5825124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542350980	chr8:5825124-5825125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7815072	chr8:5825125-5825126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561057268	chr8:5825130-5825131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113424405	chr8:5825150-5825151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546580005	chr8:5825158-5825159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571116806	chr8:5825167-5825168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116920292	chr8:5825168-5825169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552099421	chr8:5825183-5825184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570291543	chr8:5825184-5825185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189591470	chr8:5825189-5825190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2700797	chr8:5825194-5825195	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs149383994	chr8:5825230-5825231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534760624	chr8:5825239-5825240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34615837	chr8:5825247-5825248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs559943719	chr8:5825248-5825249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35915541	chr8:5825250-5825251	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs180932859	chr8:5825281-5825282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556825231	chr8:5825292-5825293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575163914	chr8:5825293-5825294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369783963	chr8:5825307-5825308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2703320	chr8:5825316-5825317	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs560874698	chr8:5825325-5825326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2816429	chr8:5825329-5825330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs13258226	chr8:5825330-5825331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs148466145	chr8:5825350-5825351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75040887	chr8:5825353-5825354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73515929	chr8:5825402-5825403	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs544208702	chr8:5825413-5825414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549556476	chr8:5825434-5825435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567712710	chr8:5825450-5825451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:130)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Type 2 diabetes	21526130	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20688739	CNVD
Osteosarcoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5821800-5827000	Weak transcription	Fetal Lung	lung
2	chr8:5822200-5826600	Weak transcription	Fetal Heart	heart
3	chr8:5826600-5827400	Flanking Active TSS	Fetal Heart	heart
4	chr8:5827000-5827400	Enhancers	Fetal Lung	lung
5	chr8:5827000-5828200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr8:5827200-5828000	Enhancers	Fetal Muscle Leg	muscle
7	chr8:5827400-5828600	Enhancers	Fetal Heart	heart
8	chr8:5827600-5827800	Enhancers	Fetal Stomach	stomach
9	chr8:5828000-5828200	Enhancers	Liver	Liver
10	chr8:5828600-5830400	Weak transcription	Fetal Heart	heart
11	chr8:5830400-5831200	Enhancers	Fetal Heart	heart
12	chr8:5847200-5847600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:5847800-5848200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:5858800-5860000	Enhancers	Placenta Amnion	Placenta Amnion
15	chr8:5859000-5859400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:5860000-5860600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr8:5863000-5870200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:5865600-5866200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr8:5865600-5866200	Enhancers	Fetal Heart	heart
20	chr8:5865600-5866200	Enhancers	Hela-S3	cervix
21	chr8:5865800-5866200	Enhancers	H9 Cell Line	embryonic stem cell
22	chr8:5865800-5866200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr8:5866000-5866200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:5866200-5875000	Weak transcription	Hela-S3	cervix
25	chr8:5866600-5869400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:5869400-5870400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:5870200-5870400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr8:5871200-5871600	Enhancers	NHEK	skin
29	chr8:5871400-5871600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:5871600-5872200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr8:5871600-5875000	Weak transcription	NHEK	skin
32	chr8:5872200-5872400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr8:5872400-5875000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr8:5872800-5874000	Enhancers	Fetal Brain Male	brain
35	chr8:5874000-5875000	Weak transcription	Fetal Brain Male	brain
36	chr8:5874400-5876800	Enhancers	Fetal Heart	heart
37	chr8:5874600-5874800	Enhancers	Aorta	Aorta
38	chr8:5874600-5876000	Enhancers	Fetal Muscle Leg	muscle
39	chr8:5874800-5875800	Weak transcription	Aorta	Aorta
40	chr8:5874800-5876000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:5874800-5876400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr8:5874800-5876600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:5874800-5876600	Enhancers	HMEC	breast
44	chr8:5875000-5875800	Enhancers	Fetal Brain Male	brain
45	chr8:5875000-5876600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr8:5875000-5878200	Enhancers	NHEK	skin
47	chr8:5875000-5878800	Enhancers	HUVEC	blood vessel
48	chr8:5875000-5879000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:5875000-5879800	Enhancers	Hela-S3	cervix
50	chr8:5875200-5875600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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