Variant report

Variant	esv1804436
Chromosome Location	chr8:58113182-58141141
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:863)
CpG islands
(count:1769)
Chromatin interactive
region (count:24)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:863 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58137879-58138528	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:58122168-58122783	HepG2	liver:	n/a	n/a
3	ATF1	chr8:58122169-58123010	K562	blood:	n/a	n/a
4	ATF3	chr8:58137924-58138390	A549	lung:	n/a	n/a
5	BACH1	chr8:58122347-58122997	K562	blood:	n/a	n/a
6	BHLHE40	chr8:58118159-58118698	K562	blood:	n/a	n/a
7	BHLHE40	chr8:58127590-58127948	K562	blood:	n/a	n/a
8	BHLHE40	chr8:58137964-58138275	HepG2	liver:	n/a	n/a
9	BHLHE40	chr8:58122112-58123036	K562	blood:	n/a	n/a
10	BRCA1	chr8:58122208-58123016	GM12878	blood:	n/a	n/a
11	BRCA1	chr8:58127438-58127751	HepG2	liver:	n/a	n/a
12	BRCA1	chr8:58118301-58118654	GM12878	blood:	n/a	n/a
13	BRCA1	chr8:58122170-58122971	HepG2	liver:	n/a	n/a
14	BRCA1	chr8:58127563-58127875	GM12878	blood:	n/a	n/a
15	CEBPB	chr8:58138106-58138233	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:58138094-58138305	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:58135434-58135802	A549	lung:	n/a	chr8:58135609-58135620
18	CEBPB	chr8:58118253-58118637	K562	blood:	n/a	chr8:58118437-58118448
19	CEBPB	chr8:58122125-58123045	K562	blood:	n/a	n/a
20	CEBPB	chr8:58135497-58135726	HepG2	liver:	n/a	chr8:58135609-58135620
21	CEBPB	chr8:58138061-58138288	A549	lung:	n/a	n/a
22	CEBPB	chr8:58137953-58138466	A549	lung:	n/a	n/a
23	CEBPB	chr8:58135426-58135823	K562	blood:	n/a	chr8:58135609-58135620
24	CEBPB	chr8:58135434-58135730	K562	blood:	n/a	chr8:58135609-58135620
25	CEBPB	chr8:58135438-58135794	Hela-S3	cervix:	n/a	chr8:58135609-58135620
26	CEBPB	chr8:58135416-58135803	HepG2	liver:	n/a	chr8:58135609-58135620
27	CEBPB	chr8:58135367-58135856	MCF-7	breast:	n/a	chr8:58135609-58135620
28	CEBPB	chr8:58135407-58135877	A549	lung:	n/a	chr8:58135609-58135620
29	CEBPB	chr8:58137871-58138537	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr8:58135455-58135719	HepG2	liver:	n/a	chr8:58135609-58135620
31	CEBPB	chr8:58118292-58118614	HepG2	liver:	n/a	chr8:58118437-58118448
32	CEBPB	chr8:58135428-58135788	IMR90	lung:	n/a	chr8:58135609-58135620
33	CEBPB	chr8:58135419-58135810	K562	blood:	n/a	chr8:58135609-58135620
34	CEBPB	chr8:58135395-58135845	MCF-7	breast:	n/a	chr8:58135609-58135620
35	CEBPD	chr8:58135517-58135669	HepG2	liver:	n/a	n/a
36	CEBPZ	chr8:58118279-58118527	HepG2	liver:	n/a	n/a
37	CHD1	chr8:58122169-58123189	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr8:58118485-58118679	GM12878	blood:	n/a	n/a
39	CHD2	chr8:58122614-58122989	GM12878	blood:	n/a	n/a
40	CHD2	chr8:58122153-58122987	K562	blood:	n/a	n/a
41	CHD2	chr8:58116729-58116763	K562	blood:	n/a	n/a
42	CHD2	chr8:58122268-58123011	HepG2	liver:	n/a	n/a
43	CHD2	chr8:58118259-58118697	HepG2	liver:	n/a	n/a
44	CHD2	chr8:58127562-58127861	HepG2	liver:	n/a	n/a
45	CTCF	chr8:58122180-58122330	GM12864	blood:	n/a	n/a
46	CTCF	chr8:58136040-58136190	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:58118480-58118630	HAc	cerebellar:	n/a	n/a
48	CTCF	chr8:58122200-58122350	AG09309	skin:	n/a	n/a
49	CTCF	chr8:58122200-58122350	GM12871	blood:	n/a	n/a
50	CTCF	chr8:58122840-58122990	AG04449	skin:	n/a	n/a

(count:1769 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58132446-58132496	AG09309	skin:	n/a
2	chr8:58132656-58132706	GM12878	blood:	n/a
3	chr8:58131602-58131652	MCF10A-Er-Src	breast:	n/a
4	chr8:58120465-58120515	ECC-1	luminal epithelium:	n/a
5	chr8:58132229-58132279	GM12891	blood:	n/a
6	chr8:58117687-58117737	CMK	blood:	n/a
7	chr8:58126962-58127012	AG04449	skin:	fetal
8	chr8:58130467-58130517	CMK	blood:	n/a
9	chr8:58138048-58138098	GM19239	blood:	n/a
10	chr8:58132656-58132706	HUVEC	blood vessel:	n/a
11	chr8:58126962-58127012	HRPEpiC	eye:	n/a
12	chr8:58119141-58119191	Caco-2	colon:	n/a
13	chr8:58117541-58117591	ECC-1	luminal epithelium:	n/a
14	chr8:58130323-58130373	HCT-116	colon:	n/a
15	chr8:58118711-58118761	GM19239	blood:	n/a
16	chr8:58130041-58130091	BJ	skin:	n/a
17	chr8:58130041-58130091	T-47D	breast:	n/a
18	chr8:58117541-58117591	HIPEpiC	eye:	n/a
19	chr8:58117541-58117591	AoSMC	blood vessel:	n/a
20	chr8:58130323-58130373	PrEC	prostate:	n/a
21	chr8:58121215-58121265	GM06990	blood:	n/a
22	chr8:58122215-58122265	HNPCEpiC	eye:	n/a
23	chr8:58132446-58132496	K562	blood:	n/a
24	chr8:58132229-58132279	BE2_C	brain:	n/a
25	chr8:58117687-58117737	PFSK-1	brain:	n/a
26	chr8:58116908-58116958	HEEpiC	esophagus:	n/a
27	chr8:58130467-58130517	AG10803	skin:	n/a
28	chr8:58130323-58130373	U87	brain:	n/a
29	chr8:58117125-58117175	HCF	heart:	n/a
30	chr8:58130467-58130517	AG09309	skin:	n/a
31	chr8:58132656-58132706	HRCEpiC	kidney:	n/a
32	chr8:58114915-58114965	Caco-2	colon:	n/a
33	chr8:58138048-58138098	SK-N-SH	brain:	n/a
34	chr8:58132287-58132337	IMR90	lung:	fetal
35	chr8:58130323-58130373	Jurkat	blood:	n/a
36	chr8:58121215-58121265	HIPEpiC	eye:	n/a
37	chr8:58132287-58132337	HepG2	liver:	n/a
38	chr8:58128466-58128516	PrEC	prostate:	n/a
39	chr8:58118711-58118761	MCF10A-Er-Src	breast:	n/a
40	chr8:58132446-58132496	PrEC	prostate:	n/a
41	chr8:58122215-58122265	AG04450	lung:	fetal
42	chr8:58120465-58120515	MCF-7	breast:	n/a
43	chr8:58128724-58128774	HepG2	liver:	n/a
44	chr8:58128466-58128516	SAEC	small airway:	n/a
45	chr8:58116908-58116958	HMEC	breast:	n/a
46	chr8:58117541-58117591	BE2_C	brain:	n/a
47	chr8:58122215-58122265	GM12891	blood:	n/a
48	chr8:58114950-58115000	SK-N-SH_RA	brain:	n/a
49	chr8:58115012-58115062	NHDF-neo	bronchial:	n/a
50	chr8:58129604-58129654	MCF-7	breast:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
2	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
3	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
4	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
5	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
6	chr8:58134015..58136749-chr8:58138139..58140095,2	K562	blood:
7	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
8	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
9	chr8:58137967..58139990-chr8:58271314..58273259,2	MCF-7	breast:
10	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
11	chr8:58129899..58132563-chr8:58137038..58139171,2	K562	blood:
12	chr8:58137340..58139312-chr8:58141710..58144515,2	MCF-7	breast:
13	chr8:58121826..58122902-chr8:58255580..58256503,3	MCF-7	breast:
14	chr8:58094506..58095013-chr8:58135741..58136318,2	MCF-7	breast:
15	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
16	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
17	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
18	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
19	chr8:58135656..58136628-chr8:58255573..58256399,7	MCF-7	breast:
20	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
21	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
22	chr8:58134015..58136749-chr8:58138139..58140095,2	K562	blood:
23	chr8:58122191..58122786-chr8:58255142..58256110,2	K562	blood:
24	chr8:58129429..58131931-chr8:58132415..58133992,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-8	chr8:58135154-58135255	NONHSAT126742
2	lnc-FAM110B-8	chr8:58131969-58132182	ENSG00000253301.1
3	lnc-FAM110B-8	chr8:58132670-58132854	ENSG00000253301.1
4	lnc-FAM110B-8	chr8:58135154-58135255	NONHSAT126741
5	lnc-FAM110B-8	chr8:58131648-58131697	ENSG00000253301.1
6	lnc-FAM110B-8	chr8:58136443-58136530	NONHSAT126744
7	lnc-FAM110B-8	chr8:58133148-58133297	ENSG00000253301.1
8	lnc-FAM110B-8	chr8:58131938-58132182	ENSG00000253301.1
9	lnc-FAM110B-8	chr8:58131648-58131697	NONHSAT126741
10	lnc-FAM110B-8	chr8:58132670-58132795	ENSG00000253301.1
11	lnc-FAM110B-8	chr8:58131162-58131254	ENSG00000253301.1
12	lnc-FAM110B-8	chr8:58135154-58135255	ENSG00000253301.1
13	lnc-FAM110B-8	chr8:58132670-58132854	ENSG00000253301.1
14	lnc-FAM110B-8	chr8:58139050-58139184	NONHSAT126742
15	lnc-FAM110B-8	chr8:58133958-58134166	ENSG00000253301.1
16	lnc-FAM110B-8	chr8:58130835-58130911	ENSG00000253301.1
17	lnc-FAM110B-8	chr8:58135154-58135255	ENSG00000253301.1
18	lnc-FAM110B-8	chr8:58134728-58134830	NONHSAT126741
19	lnc-FAM110B-8	chr8:58121058-58121191	ENSG00000253301.1
20	lnc-FAM110B-8	chr8:58131969-58132126	ENSG00000253301.1
21	lnc-FAM110B-8	chr8:58131885-58132182	NONHSAT126742
22	lnc-FAM110B-8	chr8:58133958-58134166	NONHSAT126741
23	lnc-FAM110B-8	chr8:58132670-58132854	NONHSAT126741
24	lnc-FAM110B-8	chr8:58131093-58131254	ENSG00000253301.1
25	lnc-FAM110B-8	chr8:58131969-58132182	NONHSAT126741
26	lnc-FAM110B-8	chr8:58120568-58120763	ENSG00000253301.1
27	lnc-FAM110B-8	chr8:58134728-58134830	ENSG00000253301.1
28	lnc-FAM110B-8	chr8:58131615-58131697	ENSG00000253301.1
29	lnc-FAM110B-8	chr8:58132670-58132854	NONHSAT126742
30	lnc-FAM110B-8	chr8:58131969-58132082	ENSG00000253301.1

No data

Variant related genes	Relation type
ENSG00000253301	TF binding region
ENSG00000253301	CpG island
ENSG00000253301	chromatin interactions
ENSG00000253871	chromatin interactions

Extended variants
information (count: 1766 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1766 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576528798	chr8:58113225-58113226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs2101864	chr8:58113226-58113227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs556108431	chr8:58113254-58113255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73603888	chr8:58113255-58113256	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs141164753	chr8:58113281-58113282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569235668	chr8:58113292-58113293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564200967	chr8:58113293-58113294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540635843	chr8:58113305-58113306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181732566	chr8:58113309-58113310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs16921843	chr8:58113338-58113339	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs75508377	chr8:58113348-58113349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150318938	chr8:58113357-58113358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548815076	chr8:58113368-58113369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377091592	chr8:58113408-58113409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374023348	chr8:58113416-58113417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559431767	chr8:58113428-58113429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528424243	chr8:58113438-58113439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528279715	chr8:58113439-58113440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530096017	chr8:58113442-58113443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551320718	chr8:58113466-58113467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs56211106	chr8:58113497-58113498	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs373810218	chr8:58113500-58113501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74957933	chr8:58113529-58113530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570026095	chr8:58113535-58113536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150913578	chr8:58113537-58113538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17331850	chr8:58113538-58113539	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs556025510	chr8:58113549-58113550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111657335	chr8:58113554-58113555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535207327	chr8:58113560-58113561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558038687	chr8:58113589-58113590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578134632	chr8:58113622-58113623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs137989571	chr8:58113674-58113675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563045095	chr8:58113712-58113713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12678187	chr8:58113766-58113767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs542254855	chr8:58113823-58113824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190315529	chr8:58113843-58113844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368765928	chr8:58113844-58113845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528402887	chr8:58113853-58113854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6995355	chr8:58113870-58113871	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs557270917	chr8:58113922-58113923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182579012	chr8:58113924-58113925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575844583	chr8:58113929-58113930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6995378	chr8:58113933-58113934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs535842360	chr8:58113938-58113939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6981055	chr8:58113941-58113942	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs149606622	chr8:58113973-58113974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534971270	chr8:58113980-58113981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72621430	chr8:58113984-58113985	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs187076781	chr8:58114002-58114003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537294447	chr8:58114005-58114006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58106200-58114800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:58114800-58115400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:58115400-58118200	Weak transcription	Right Atrium	heart
4	chr8:58116000-58117400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:58116200-58117000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:58116200-58117200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:58116400-58117000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
10	chr8:58116400-58117200	ZNF genes & repeats	Spleen	Spleen
11	chr8:58116400-58117400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
12	chr8:58116400-58118000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr8:58116600-58116800	ZNF genes & repeats	Brain Hippocampus Middle	brain
14	chr8:58116600-58117000	Enhancers	Gastric	stomach
15	chr8:58116600-58117200	ZNF genes & repeats	Fetal Kidney	kidney
16	chr8:58116600-58117200	ZNF genes & repeats	Pancreas	Pancrea
17	chr8:58116600-58117600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:58116600-58118800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr8:58116800-58118200	Weak transcription	Brain Hippocampus Middle	brain
20	chr8:58117000-58118200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:58117000-58118200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:58117000-58118200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr8:58117000-58118200	Weak transcription	Gastric	stomach
24	chr8:58117000-58119000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr8:58117200-58118200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:58117200-58118200	Weak transcription	Fetal Kidney	kidney
27	chr8:58117400-58118200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:58117800-58118800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
29	chr8:58118000-58118800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
30	chr8:58118000-58118800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr8:58118000-58118800	ZNF genes & repeats	Brain Germinal Matrix	brain
32	chr8:58118000-58118800	ZNF genes & repeats	Pancreas	Pancrea
33	chr8:58118200-58118400	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
34	chr8:58118200-58118600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
35	chr8:58118200-58118600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
36	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Large	intestine
37	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Small	intestine
38	chr8:58118200-58118600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
39	chr8:58118200-58118600	ZNF genes & repeats	Placenta	Placenta
40	chr8:58118200-58118600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
41	chr8:58118200-58118600	ZNF genes & repeats	NHEK	skin
42	chr8:58118200-58118800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
43	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:58118200-58118800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr8:58118200-58118800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:58118200-58118800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
48	chr8:58118200-58118800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
49	chr8:58118200-58118800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
50	chr8:58118200-58118800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell

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