Variant report

Variant	nsv1031245
Chromosome Location	chr8:111716585-111875753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1152)
CpG islands
(count:305)
Chromatin interactive
region (count:37)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1152 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:111844737-111844834	K562	blood:	n/a	n/a
2	ARID3A	chr8:111842727-111843064	K562	blood:	n/a	n/a
3	ARID3A	chr8:111842737-111843081	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:111861128-111861289	K562	blood:	n/a	n/a
5	ARID3A	chr8:111844706-111844955	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:111860419-111860636	K562	blood:	n/a	n/a
7	ARID3A	chr8:111860272-111860903	HepG2	liver:	n/a	chr8:111860332-111860348
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	chr8:111758677-111758916	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr8:111758735-111758917	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	chr8:111810832-111811007	K562	blood:	n/a	n/a
20	CBX3	chr8:111810769-111811126	K562	blood:	n/a	n/a
21	CEBPB	chr8:111769556-111769845	A549	lung:	n/a	chr8:111769695-111769706
22	CEBPB	chr8:111758683-111758901	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr8:111757204-111757296	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:111867670-111867880	MCF-7	breast:	n/a	chr8:111867774-111867785
25	CEBPB	chr8:111856388-111856588	HepG2	liver:	n/a	chr8:111856520-111856532
26	CEBPB	chr8:111793925-111794261	A549	lung:	n/a	n/a
27	CEBPB	chr8:111769516-111769877	H1-hESC	embryonic stem cell:	n/a	chr8:111769695-111769706
28	CEBPB	chr8:111769530-111769868	HepG2	liver:	n/a	chr8:111769695-111769706
29	CEBPB	chr8:111793930-111794262	HepG2	liver:	n/a	n/a
30	CEBPB	chr8:111769540-111769842	Hela-S3	cervix:	n/a	chr8:111769695-111769706
31	CEBPB	chr8:111724257-111724440	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:111793912-111794250	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:111867668-111867906	HepG2	liver:	n/a	chr8:111867774-111867785
34	CEBPB	chr8:111856485-111856584	A549	lung:	n/a	chr8:111856520-111856532
35	CEBPB	chr8:111794027-111794161	K562	blood:	n/a	n/a
36	CEBPB	chr8:111755449-111755533	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:111769522-111769876	IMR90	lung:	n/a	chr8:111769695-111769706
38	CEBPB	chr8:111856639-111856677	K562	blood:	n/a	n/a
39	CEBPB	chr8:111847032-111847354	IMR90	lung:	n/a	n/a
40	CEBPB	chr8:111816593-111816629	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:111793909-111794206	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr8:111726278-111726443	GM12878	blood:	n/a	n/a
43	CHD2	chr8:111847633-111848502	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr8:111758688-111758879	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr8:111872571-111872576	HepG2	liver:	n/a	n/a
46	CREB1	chr8:111847735-111848094	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr8:111834389-111834599	HepG2	liver:	n/a	n/a
48	CTCF	chr8:111842640-111842790	AG04450	lung:	n/a	n/a
49	CTCF	chr8:111844720-111844870	HL-60	blood:	n/a	n/a
50	CTCF	chr8:111844719-111844837	GM19238	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:111834906-111834956	NT2-D1	testis:	n/a
2	chr8:111835043-111835093	HIPEpiC	eye:	n/a
3	chr8:111834906-111834956	HMEC	breast:	n/a
4	chr8:111834752-111834802	NT2-D1	testis:	n/a
5	chr8:111834776-111834826	AG09309	skin:	n/a
6	chr8:111834776-111834826	SK-N-SH	brain:	n/a
7	chr8:111847388-111847438	HAEpiC	amniotic membrane:	n/a
8	chr8:111834776-111834826	HIPEpiC	eye:	n/a
9	chr8:111834906-111834956	MCF10A-Er-Src	breast:	n/a
10	chr8:111834906-111834956	RPTEC	kidney:	n/a
11	chr8:111834776-111834826	ProgFib	skin:	n/a
12	chr8:111847388-111847438	AG04449	skin:	fetal
13	chr8:111847388-111847438	HEK293	kidney:	embryo
14	chr8:111847388-111847438	Caco-2	colon:	n/a
15	chr8:111834906-111834956	HUVEC	blood vessel:	n/a
16	chr8:111834906-111834956	HCM	heart:	n/a
17	chr8:111835043-111835093	PFSK-1	brain:	n/a
18	chr8:111834752-111834802	AoSMC	blood vessel:	n/a
19	chr8:111834752-111834802	NHBE	bronchial:	n/a
20	chr8:111847388-111847438	HRE	kidney:	n/a
21	chr8:111847388-111847438	HNPCEpiC	eye:	n/a
22	chr8:111847388-111847438	U87	brain:	n/a
23	chr8:111847388-111847438	MCF10A-Er-Src	breast:	n/a
24	chr8:111834906-111834956	PANC-1	pancreas:	n/a
25	chr8:111834776-111834826	HAEpiC	amniotic membrane:	n/a
26	chr8:111834752-111834802	AG04449	skin:	fetal
27	chr8:111835043-111835093	AG09319	gingival:	n/a
28	chr8:111834752-111834802	U87	brain:	n/a
29	chr8:111834906-111834956	HNPCEpiC	eye:	n/a
30	chr8:111847388-111847438	NT2-D1	testis:	n/a
31	chr8:111834752-111834802	ProgFib	skin:	n/a
32	chr8:111835043-111835093	LNCaP	prostate:	n/a
33	chr8:111834752-111834802	RPTEC	kidney:	n/a
34	chr8:111835043-111835093	GM12891	blood:	n/a
35	chr8:111835043-111835093	Jurkat	blood:	n/a
36	chr8:111834752-111834802	HUVEC	blood vessel:	n/a
37	chr8:111834752-111834802	GM19239	blood:	n/a
38	chr8:111834906-111834956	T-47D	breast:	n/a
39	chr8:111834776-111834826	SK-N-SH_RA	brain:	n/a
40	chr8:111835043-111835093	HCT-116	colon:	n/a
41	chr8:111834752-111834802	HEEpiC	esophagus:	n/a
42	chr8:111847388-111847438	RPTEC	kidney:	n/a
43	chr8:111847388-111847438	SKMC	muscle:	n/a
44	chr8:111834752-111834802	HL-60	blood:	n/a
45	chr8:111834906-111834956	SK-N-MC	brain:	n/a
46	chr8:111834752-111834802	GM12878	blood:	n/a
47	chr8:111847388-111847438	A549	lung:	n/a
48	chr8:111834752-111834802	HMEC	breast:	n/a
49	chr8:111834776-111834826	CMK	blood:	n/a
50	chr8:111847388-111847438	AG09319	gingival:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:77766844..77769049-chr8:111860348..111862470,2	MCF-7	breast:
2	chr6:47444917..47447011-chr8:111717811..111719807,2	MCF-7	breast:
3	chr8:111780743..111782594-chr8:111785721..111788222,2	MCF-7	breast:
4	chr8:111705966..111708208-chr8:111719733..111721854,2	MCF-7	breast:
5	chr8:111712144..111713669-chr8:111724852..111727560,2	MCF-7	breast:
6	chr8:111365378..111366118-chr8:111834050..111834594,2	MCF-7	breast:
7	chr8:111770515..111773370-chr8:111778420..111781176,2	K562	blood:
8	chr8:111842914..111844843-chr8:111916183..111918986,2	MCF-7	breast:
9	chr8:111714002..111715922-chr8:111718938..111720595,2	K562	blood:
10	chr8:111744937..111746990-chr8:111753666..111755908,2	K562	blood:
11	chr8:111811884..111813878-chr8:111822855..111824615,2	K562	blood:
12	chr8:111781609..111784016-chr8:111789603..111791637,2	MCF-7	breast:
13	chr8:111870941..111873511-chr8:111873961..111876570,2	K562	blood:
14	chr8:111365137..111367407-chr8:111844337..111845381,8	MCF-7	breast:
15	chr8:111815829..111818454-chr8:111818863..111820532,2	K562	blood:
16	chr8:111781609..111784016-chr8:111789603..111791637,2	MCF-7	breast:
17	chr8:111799556..111802962-chr8:111805139..111808019,3	MCF-7	breast:
18	chr8:111811884..111813878-chr8:111822855..111824615,2	K562	blood:
19	chr8:111059646..111060573-chr8:111844351..111844977,3	MCF-7	breast:
20	chr8:111870941..111873511-chr8:111873961..111876570,2	K562	blood:
21	chr8:111059529..111060611-chr8:111844370..111845275,3	MCF-7	breast:
22	chr8:111744937..111746990-chr8:111753666..111755908,2	K562	blood:
23	chr8:111661559..111663835-chr8:111734745..111737537,2	MCF-7	breast:
24	chr8:111148225..111150967-chr8:111837407..111839836,2	MCF-7	breast:
25	chr8:111731408..111733781-chr8:111735894..111737971,2	K562	blood:
26	chr8:111799556..111802962-chr8:111805139..111808019,3	MCF-7	breast:
27	chr8:111365308..111365953-chr8:111842805..111843518,2	MCF-7	breast:
28	chr8:111780743..111782594-chr8:111785721..111788222,2	MCF-7	breast:
29	chr8:111853597..111856569-chr8:111856769..111860452,3	MCF-7	breast:
30	chr8:111842460..111843306-chr8:121617683..121618475,2	MCF-7	breast:
31	chr8:111846862..111847654-chr8:112265014..112265719,2	MCF-7	breast:
32	chr8:111855787..111857322-chr8:111859376..111860898,2	MCF-7	breast:
33	chr8:110746955..110747968-chr8:111842364..111843455,3	MCF-7	breast:
34	chr8:111731408..111733781-chr8:111735894..111737971,2	K562	blood:
35	chr8:111855787..111857322-chr8:111859376..111860898,2	MCF-7	breast:
36	chr8:111815829..111818454-chr8:111818863..111820532,2	K562	blood:
37	chr8:111853597..111856569-chr8:111856769..111860452,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-3	chr8:111779092-111779145	ENSG00000253717
2	lnc-RP11-422N16.3.1-3	chr8:111784567-111784988	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
ENSG00000270761	chromatin interactions
ENSG00000198087	chromatin interactions
ENSG00000253717	chromatin interactions

Extended variants
information (count: 3636 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3636 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373232277	chr8:111716604-111716605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535588111	chr8:111716613-111716614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558409806	chr8:111716622-111716623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77488081	chr8:111716658-111716659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572070722	chr8:111716669-111716670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375875224	chr8:111716678-111716679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544719547	chr8:111716731-111716732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534353916	chr8:111716756-111716757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190374962	chr8:111716779-111716780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577964018	chr8:111716805-111716806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560004225	chr8:111716871-111716872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543698215	chr8:111716876-111716877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563599266	chr8:111716889-111716890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571991061	chr8:111716904-111716905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543178834	chr8:111716963-111716964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78562896	chr8:111716993-111716994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528572139	chr8:111717049-111717050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551514984	chr8:111717064-111717065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572340571	chr8:111717168-111717169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564590371	chr8:111717264-111717265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200689976	chr8:111717281-111717282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201778569	chr8:111717282-111717283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533309494	chr8:111717285-111717286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140470319	chr8:111717291-111717292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550099629	chr8:111717314-111717315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73702328	chr8:111717356-111717357	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs535303622	chr8:111717368-111717369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75457378	chr8:111717388-111717389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181526035	chr8:111717390-111717391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534712224	chr8:111717432-111717433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148082284	chr8:111717456-111717457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35833852	chr8:111717481-111717482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369291906	chr8:111717486-111717487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374685644	chr8:111717487-111717488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs74450696	chr8:111717488-111717489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577227689	chr8:111717494-111717495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536602034	chr8:111717495-111717496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557254565	chr8:111717505-111717506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561047399	chr8:111717535-111717536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141375446	chr8:111717580-111717581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542888008	chr8:111717594-111717595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540699534	chr8:111717625-111717626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548570162	chr8:111717635-111717636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529872419	chr8:111717639-111717640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573306562	chr8:111717654-111717655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187566934	chr8:111717682-111717683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565328565	chr8:111717687-111717688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs75954526	chr8:111717722-111717723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189164422	chr8:111717724-111717725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181843290	chr8:111717726-111717727	Enhancers	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:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111716600-111717400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:111717200-111717600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr8:111717400-111718400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:111726000-111726200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:111726200-111729600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:111729600-111729800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:111739400-111740200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:111739800-111740200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:111739800-111740400	Enhancers	Adipose Nuclei	Adipose
10	chr8:111743800-111744200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:111743800-111744400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr8:111745600-111749000	Weak transcription	Spleen	Spleen
13	chr8:111758400-111758800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr8:111758800-111759200	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr8:111759200-111759800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr8:111759400-111759800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:111764000-111764600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr8:111764200-111764800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr8:111768400-111769600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:111769200-111770000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr8:111769400-111769800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr8:111769400-111769800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr8:111769400-111769800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr8:111772200-111772600	Active TSS	Aorta	Aorta
25	chr8:111784800-111785600	Enhancers	Fetal Intestine Small	intestine
26	chr8:111788600-111826200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr8:111791600-111792000	Active TSS	Primary hematopoietic stem cells	blood
28	chr8:111802400-111802800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:111802800-111803200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:111803200-111804000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:111803200-111804400	Enhancers	Fetal Intestine Large	intestine
32	chr8:111803400-111804200	Enhancers	Fetal Intestine Small	intestine
33	chr8:111804000-111804400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:111814600-111815200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:111814600-111815200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr8:111814800-111815400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr8:111815000-111815200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr8:111815000-111815400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr8:111818600-111818800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr8:111818600-111819600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr8:111818800-111819400	Enhancers	Adipose Nuclei	Adipose
42	chr8:111818800-111819800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:111818800-111821000	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr8:111820200-111821000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:111820600-111821000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr8:111821000-111821400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:111821000-111821600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr8:111821000-111822400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:111821400-111822200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:111821600-111822000	Enhancers	HUES6 Cell Line	embryonic stem cell

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