Variant report

Variant	nsv831423
Chromosome Location	chr8:111672801-111869818
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1247)
CpG islands
(count:367)
Chromatin interactive
region (count:52)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1247 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:111842727-111843064	K562	blood:	n/a	n/a
2	ARID3A	chr8:111844706-111844955	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:111860419-111860636	K562	blood:	n/a	n/a
4	ARID3A	chr8:111842737-111843081	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:111860272-111860903	HepG2	liver:	n/a	chr8:111860332-111860348
6	ARID3A	chr8:111844737-111844834	K562	blood:	n/a	n/a
7	ARID3A	chr8:111861128-111861289	K562	blood:	n/a	n/a
8	ATF1	chr8:111804441-111804627	K562	blood:	n/a	n/a
9	ATF2	chr8:111758671-111758920	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr8:111758640-111758925	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr8:111860291-111860669	K562	blood:	n/a	n/a
12	BACH1	chr8:111719799-111719982	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr8:111860419-111860570	GM12878	blood:	n/a	chr8:111860544-111860554
14	BCL11A	chr8:111758735-111758917	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr8:111758677-111758916	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr8:111719822-111720092	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:111842552-111842735	K562	blood:	n/a	n/a
18	BRCA1	chr8:111846598-111846609	HepG2	liver:	n/a	n/a
19	CBX3	chr8:111810769-111811126	K562	blood:	n/a	n/a
20	CBX3	chr8:111810832-111811007	K562	blood:	n/a	n/a
21	CEBPB	chr8:111769540-111769842	Hela-S3	cervix:	n/a	chr8:111769695-111769706
22	CEBPB	chr8:111769516-111769877	H1-hESC	embryonic stem cell:	n/a	chr8:111769695-111769706
23	CEBPB	chr8:111793912-111794250	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:111816593-111816629	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:111769522-111769876	IMR90	lung:	n/a	chr8:111769695-111769706
26	CEBPB	chr8:111793930-111794262	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:111708632-111709146	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:111708552-111709216	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:111688332-111688445	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr8:111793925-111794261	A549	lung:	n/a	n/a
31	CEBPB	chr8:111793909-111794206	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr8:111769530-111769868	HepG2	liver:	n/a	chr8:111769695-111769706
33	CEBPB	chr8:111678139-111678458	HepG2	liver:	n/a	chr8:111678273-111678284
34	CEBPB	chr8:111714073-111714166	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr8:111755449-111755533	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr8:111856388-111856588	HepG2	liver:	n/a	chr8:111856520-111856532
37	CEBPB	chr8:111757204-111757296	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:111758683-111758901	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:111684904-111685112	IMR90	lung:	n/a	n/a
40	CEBPB	chr8:111856639-111856677	K562	blood:	n/a	n/a
41	CEBPB	chr8:111724257-111724440	HepG2	liver:	n/a	n/a
42	CEBPB	chr8:111867670-111867880	MCF-7	breast:	n/a	chr8:111867774-111867785
43	CEBPB	chr8:111794027-111794161	K562	blood:	n/a	n/a
44	CEBPB	chr8:111856485-111856584	A549	lung:	n/a	chr8:111856520-111856532
45	CEBPB	chr8:111673382-111673531	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:111847032-111847354	IMR90	lung:	n/a	n/a
47	CEBPB	chr8:111688373-111688402	K562	blood:	n/a	n/a
48	CEBPB	chr8:111678183-111678436	A549	lung:	n/a	chr8:111678273-111678284
49	CEBPB	chr8:111769556-111769845	A549	lung:	n/a	chr8:111769695-111769706
50	CEBPB	chr8:111867668-111867906	HepG2	liver:	n/a	chr8:111867774-111867785

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:111847388-111847438	GM19239	blood:	n/a
2	chr8:111847388-111847438	GM19239	blood:	n/a
3	chr8:111847388-111847438	HMEC	breast:	n/a
4	chr8:111835043-111835093	K562	blood:	n/a
5	chr8:111834752-111834802	GM19239	blood:	n/a
6	chr8:111847388-111847438	HCM	heart:	n/a
7	chr8:111707758-111707808	T-47D	breast:	n/a
8	chr8:111834752-111834802	HCF	heart:	n/a
9	chr8:111834752-111834802	SKMC	muscle:	n/a
10	chr8:111834776-111834826	HUVEC	blood vessel:	n/a
11	chr8:111847388-111847438	Hepatocyte	liver:	n/a
12	chr8:111834906-111834956	HEEpiC	esophagus:	n/a
13	chr8:111834752-111834802	PANC-1	pancreas:	n/a
14	chr8:111707758-111707808	SK-N-MC	brain:	n/a
15	chr8:111835043-111835093	Hela-S3	cervix:	n/a
16	chr8:111834776-111834826	HMEC	breast:	n/a
17	chr8:111834776-111834826	HepG2	liver:	n/a
18	chr8:111707758-111707808	NHBE	bronchial:	n/a
19	chr8:111834906-111834956	NHDF-neo	bronchial:	n/a
20	chr8:111834752-111834802	AG09319	gingival:	n/a
21	chr8:111835043-111835093	U87	brain:	n/a
22	chr8:111834776-111834826	MCF10A-Er-Src	breast:	n/a
23	chr8:111834906-111834956	HEK293	kidney:	embryo
24	chr8:111834752-111834802	SK-N-MC	brain:	n/a
25	chr8:111834752-111834802	Caco-2	colon:	n/a
26	chr8:111707758-111707808	AoSMC	blood vessel:	n/a
27	chr8:111834752-111834802	PrEC	prostate:	n/a
28	chr8:111707758-111707808	SK-N-SH_RA	brain:	n/a
29	chr8:111835043-111835093	ovcar-3	ovarian:	n/a
30	chr8:111835043-111835093	HCT-116	colon:	n/a
31	chr8:111834906-111834956	AG09319	gingival:	n/a
32	chr8:111834906-111834956	SKMC	muscle:	n/a
33	chr8:111834906-111834956	RPTEC	kidney:	n/a
34	chr8:111834906-111834956	AG04450	lung:	fetal
35	chr8:111834776-111834826	HCT-116	colon:	n/a
36	chr8:111835043-111835093	HPAEpiC	pulmonary alveolar:	n/a
37	chr8:111834776-111834826	NH-A	brain:	n/a
38	chr8:111835043-111835093	NHBE	bronchial:	n/a
39	chr8:111847388-111847438	SK-N-MC	brain:	n/a
40	chr8:111834776-111834826	NHBE	bronchial:	n/a
41	chr8:111835043-111835093	CMK	blood:	n/a
42	chr8:111834752-111834802	NH-A	brain:	n/a
43	chr8:111834752-111834802	AG04449	skin:	fetal
44	chr8:111707758-111707808	HCT-116	colon:	n/a
45	chr8:111835043-111835093	AG04449	skin:	fetal
46	chr8:111707758-111707808	U87	brain:	n/a
47	chr8:111834752-111834802	NHBE	bronchial:	n/a
48	chr8:111835043-111835093	HUVEC	blood vessel:	n/a
49	chr8:111835043-111835093	PrEC	prostate:	n/a
50	chr8:111834752-111834802	RPTEC	kidney:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:111714002..111715922-chr8:111718938..111720595,2	K562	blood:
2	chr8:111842914..111844843-chr8:111916183..111918986,2	MCF-7	breast:
3	chr8:111059529..111060611-chr8:111844370..111845275,3	MCF-7	breast:
4	chr8:111842460..111843306-chr8:121617683..121618475,2	MCF-7	breast:
5	chr8:111780743..111782594-chr8:111785721..111788222,2	MCF-7	breast:
6	chr8:111744937..111746990-chr8:111753666..111755908,2	K562	blood:
7	chr8:111059646..111060573-chr8:111844351..111844977,3	MCF-7	breast:
8	chr8:111846862..111847654-chr8:112265014..112265719,2	MCF-7	breast:
9	chr8:111712144..111713669-chr8:111724852..111727560,2	MCF-7	breast:
10	chr8:111853597..111856569-chr8:111856769..111860452,3	MCF-7	breast:
11	chr8:111665338..111666843-chr8:111677219..111678888,2	K562	blood:
12	chr8:111365308..111365953-chr8:111842805..111843518,2	MCF-7	breast:
13	chr8:111799556..111802962-chr8:111805139..111808019,3	MCF-7	breast:
14	chr8:111365137..111367407-chr8:111844337..111845381,8	MCF-7	breast:
15	chr8:111705966..111708208-chr8:111719733..111721854,2	MCF-7	breast:
16	chr8:111689286..111692174-chr8:111701872..111704181,2	MCF-7	breast:
17	chr8:111770515..111773370-chr8:111778420..111781176,2	K562	blood:
18	chr8:110746955..110747968-chr8:111842364..111843455,3	MCF-7	breast:
19	chr8:111811884..111813878-chr8:111822855..111824615,2	K562	blood:
20	chr8:111681810..111684012-chr8:111686136..111688041,2	K562	blood:
21	chr8:111712144..111713669-chr8:111724852..111727560,2	MCF-7	breast:
22	chr8:111815829..111818454-chr8:111818863..111820532,2	K562	blood:
23	chr8:111714002..111715922-chr8:111718938..111720595,2	K562	blood:
24	chr8:111365378..111366118-chr8:111834050..111834594,2	MCF-7	breast:
25	chr8:111815829..111818454-chr8:111818863..111820532,2	K562	blood:
26	chr8:111676345..111679299-chr8:111684096..111685867,2	MCF-7	breast:
27	chr8:111689286..111692174-chr8:111701872..111704181,2	MCF-7	breast:
28	chr8:111702766..111704836-chr8:111705809..111708776,2	MCF-7	breast:
29	chr8:111853597..111856569-chr8:111856769..111860452,3	MCF-7	breast:
30	chr8:111676345..111679299-chr8:111684096..111685867,2	MCF-7	breast:
31	chr8:111705966..111708208-chr8:111719733..111721854,2	MCF-7	breast:
32	chr8:111661559..111663835-chr8:111734745..111737537,2	MCF-7	breast:
33	chr8:111855787..111857322-chr8:111859376..111860898,2	MCF-7	breast:
34	chr8:37622904..37623517-chr8:111713671..111714213,2	MCF-7	breast:
35	chr8:111731408..111733781-chr8:111735894..111737971,2	K562	blood:
36	chr8:111667414..111669906-chr8:111688361..111690572,2	MCF-7	breast:
37	chr8:111148225..111150967-chr8:111837407..111839836,2	MCF-7	breast:
38	chr8:111811884..111813878-chr8:111822855..111824615,2	K562	blood:
39	chr8:111799556..111802962-chr8:111805139..111808019,3	MCF-7	breast:
40	chr12:43241796..43242729-chr8:111709968..111710717,2	MCF-7	breast:
41	chr8:111702766..111704836-chr8:111705809..111708776,2	MCF-7	breast:
42	chr8:111744937..111746990-chr8:111753666..111755908,2	K562	blood:
43	chr8:111731408..111733781-chr8:111735894..111737971,2	K562	blood:
44	chr6:47444917..47447011-chr8:111717811..111719807,2	MCF-7	breast:
45	chr8:111681810..111684012-chr8:111686136..111688041,2	K562	blood:
46	chr11:74302754..74304460-chr8:111676552..111678415,2	MCF-7	breast:
47	chr8:111780743..111782594-chr8:111785721..111788222,2	MCF-7	breast:
48	chr8:111855787..111857322-chr8:111859376..111860898,2	MCF-7	breast:
49	chr8:111781609..111784016-chr8:111789603..111791637,2	MCF-7	breast:
50	chr8:111781609..111784016-chr8:111789603..111791637,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-3	chr8:111784567-111784988	ENSG00000253717
2	lnc-RP11-422N16.3.1-3	chr8:111779092-111779145	ENSG00000253717
3	lnc-KCNV1-5	chr8:111821623-111822123	NONHSAT128312

No data

Variant related genes	Relation type
ENSG00000253994	TF binding region
ENSG00000253717	TF binding region
ENSG00000253994	CpG island
ENSG00000253717	CpG island
ENSG00000077514	chromatin interactions
ENSG00000198087	chromatin interactions
ENSG00000270761	chromatin interactions
ENSG00000253717	chromatin interactions

Extended variants
information (count: 4757 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4757 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547959973	chr8:111672848-111672849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529253272	chr8:111672855-111672856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555278182	chr8:111672869-111672870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369099486	chr8:111672900-111672901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570949108	chr8:111672908-111672909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539899769	chr8:111672922-111672923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575075513	chr8:111672931-111672932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150800453	chr8:111672956-111672957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570005540	chr8:111673009-111673010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6983816	chr8:111673039-111673040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs373556040	chr8:111673080-111673081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554830544	chr8:111673081-111673082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574571817	chr8:111673094-111673095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540033576	chr8:111673107-111673108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553489222	chr8:111673115-111673116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185087176	chr8:111673127-111673128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545466837	chr8:111673147-111673148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138061978	chr8:111673154-111673155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531323459	chr8:111673218-111673219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542188112	chr8:111673234-111673235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143650912	chr8:111673271-111673272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527931286	chr8:111673274-111673275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147183377	chr8:111673277-111673278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571009643	chr8:111673294-111673295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533485138	chr8:111673299-111673300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188801000	chr8:111673341-111673342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73700912	chr8:111673370-111673371	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs201153381	chr8:111673383-111673384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140491445	chr8:111673440-111673441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193296620	chr8:111673444-111673445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568333626	chr8:111673477-111673478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs72674973	chr8:111673509-111673510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557421668	chr8:111673557-111673558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577224537	chr8:111673590-111673591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533793800	chr8:111673620-111673621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377251091	chr8:111673631-111673632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185552664	chr8:111673634-111673635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368928448	chr8:111673653-111673654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs720966	chr8:111673693-111673694	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs720965	chr8:111673699-111673700	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs556204231	chr8:111673701-111673702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371332283	chr8:111673711-111673712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144336262	chr8:111673781-111673782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs16880997	chr8:111673804-111673805	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs4534104	chr8:111673853-111673854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188403301	chr8:111673937-111673938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147377914	chr8:111673976-111673977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs180811940	chr8:111673991-111673992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564685166	chr8:111673993-111673994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573207383	chr8:111674048-111674049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
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
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
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111672600-111676600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:111674400-111675400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr8:111675000-111675400	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr8:111675400-111679600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr8:111676200-111677000	Enhancers	HMEC	breast
6	chr8:111676600-111677200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:111676800-111677000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:111677000-111677400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr8:111677000-111677400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr8:111677400-111677600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:111677400-111681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr8:111677600-111680800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:111679600-111680200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr8:111679600-111682800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:111680200-111681200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr8:111680800-111683000	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr8:111680800-111685400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:111681000-111683000	Enhancers	Primary hematopoietic stem cells	blood
19	chr8:111681200-111682800	Enhancers	Muscle Satellite Cultured Cells	--
20	chr8:111681200-111683200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr8:111681400-111683000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr8:111681600-111682800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr8:111681600-111683000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr8:111682200-111682600	Enhancers	HSMMtube	muscle
25	chr8:111682800-111684200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr8:111682800-111685400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:111683000-111684000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr8:111683000-111684000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr8:111683000-111684400	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr8:111683000-111685200	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr8:111683200-111683600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr8:111683600-111687400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr8:111684000-111686000	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr8:111684000-111687400	Enhancers	Primary hematopoietic stem cells	blood
35	chr8:111684200-111684800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:111684200-111685200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr8:111684400-111687400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr8:111684800-111685400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr8:111685200-111685600	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr8:111685400-111685600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:111685400-111685800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:111685400-111686600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr8:111685600-111686600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr8:111685800-111686200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:111686000-111686600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr8:111686600-111686800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr8:111686600-111687400	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr8:111686600-111687400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:111689000-111689200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:111689200-111689800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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