Variant report

Variant	esv3360687
Chromosome Location	chr8:143961080-143998221
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	BATF	chr8:143987622-143987828	GM12878	blood:	n/a	chr8:143987764-143987775
2	BHLHE40	chr8:143975332-143975632	HepG2	liver:	n/a	n/a
3	BHLHE40	chr8:143975344-143975622	K562	blood:	n/a	n/a
4	CBX3	chr8:143993340-143993685	K562	blood:	n/a	n/a
5	CEBPB	chr8:143975315-143975613	Hela-S3	cervix:	n/a	n/a
6	CHD2	chr8:143968205-143968520	K562	blood:	n/a	n/a
7	CTCF	chr8:143994622-143994697	Hela-S3	cervix:	n/a	chr8:143994656-143994665 chr8:143994632-143994645
8	CTCF	chr8:143968885-143968916	K562	blood:	n/a	n/a
9	CTCF	chr8:143994720-143994870	GM12871	blood:	n/a	n/a
10	CTCF	chr8:143994568-143994734	GM12891	blood:	n/a	chr8:143994656-143994665 chr8:143994632-143994645
11	CTCF	chr8:143994581-143994712	K562	blood:	n/a	chr8:143994656-143994665 chr8:143994632-143994645
12	CTCF	chr8:143994586-143994696	GM19238	blood:	n/a	chr8:143994656-143994665 chr8:143994632-143994645
13	CTCF	chr8:143987000-143987150	GM12875	blood:	n/a	n/a
14	CTCF	chr8:143994599-143994742	GM10248	blood:	n/a	chr8:143994656-143994665 chr8:143994632-143994645
15	CTCF	chr8:143994563-143994638	GM12892	blood:	n/a	n/a
16	CTCF	chr8:143988720-143988870	HCT-116	colon:	n/a	n/a
17	CTCF	chr8:143961678-143961759	GM20000	blood:	n/a	n/a
18	CUX1	chr8:143977763-143977837	K562	blood:	n/a	n/a
19	EBF1	chr8:143997953-143998106	GM12878	blood:	n/a	n/a
20	EBF1	chr8:143989032-143989208	GM12878	blood:	n/a	n/a
21	EBF1	chr8:143979537-143979979	GM12878	blood:	n/a	n/a
22	EGR1	chr8:143993744-143994024	K562	blood:	n/a	chr8:143993918-143993932 chr8:143993919-143993932 chr8:143993920-143993929 chr8:143993925-143993938 chr8:143993919-143993932 chr8:143993919-143993932 chr8:143993919-143993929 chr8:143993914-143993936 chr8:143993923-143993933 chr8:143993877-143993887 chr8:143993918-143993933 chr8:143993919-143993932
23	EGR1	chr8:143993819-143994054	K562	blood:	n/a	chr8:143993918-143993932 chr8:143993919-143993932 chr8:143993920-143993929 chr8:143993925-143993938 chr8:143993919-143993932 chr8:143993919-143993932 chr8:143993919-143993929 chr8:143993914-143993936 chr8:143993923-143993933 chr8:143993877-143993887 chr8:143993918-143993933 chr8:143993919-143993932
24	ELF1	chr8:143993227-143993853	MCF-7	breast:	n/a	chr8:143993487-143993500
25	ELF1	chr8:143993382-143993601	HepG2	liver:	n/a	chr8:143993487-143993500
26	ELF1	chr8:143993285-143993676	K562	blood:	n/a	chr8:143993487-143993500
27	ELK1	chr8:143983813-143983816	Hela-S3	cervix:	n/a	n/a
28	EP300	chr8:143987188-143987251	K562	blood:	n/a	n/a
29	EP300	chr8:143979443-143980098	GM12878	blood:	n/a	n/a
30	FOSL2	chr8:143979468-143980152	HepG2	liver:	n/a	n/a
31	FOXA2	chr8:143979465-143980049	A549	lung:	n/a	n/a
32	FOXP2	chr8:143983504-143983917	SK-N-MC	brain:	n/a	n/a
33	GABPA	chr8:143979778-143980075	Hela-S3	cervix:	n/a	n/a
34	GABPA	chr8:143979480-143979775	Hela-S3	cervix:	n/a	n/a
35	GATA1	chr8:143975138-143975670	PBDE	blood:	n/a	n/a
36	GATA3	chr8:143981134-143981524	T-47D	breast:	n/a	n/a
37	HCFC1	chr8:143993429-143993611	K562	blood:	n/a	n/a
38	HEY1	chr8:143979414-143980147	K562	blood:	n/a	n/a
39	IRF4	chr8:143979391-143980186	GM12878	blood:	n/a	n/a
40	IRF4	chr8:143979516-143979822	GM12878	blood:	n/a	n/a
41	JUN	chr8:143984574-143984774	K562	blood:	n/a	n/a
42	JUND	chr8:143991527-143991650	K562	blood:	n/a	n/a
43	JUND	chr8:143979829-143980089	HepG2	liver:	n/a	n/a
44	MAFK	chr8:143983696-143983813	HepG2	liver:	n/a	chr8:143983728-143983743
45	MAFK	chr8:143983704-143983817	HepG2	liver:	n/a	chr8:143983728-143983743
46	MAX	chr8:143993376-143993691	K562	blood:	n/a	n/a
47	MAX	chr8:143997252-143997468	K562	blood:	n/a	chr8:143997357-143997372
48	MAX	chr8:143997317-143997527	A549	lung:	n/a	chr8:143997357-143997372
49	MAX	chr8:143993312-143994031	MCF-7	breast:	n/a	n/a
50	MAX	chr8:143993493-143993519	NB4	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:143961341-143961391	BJ	skin:	n/a
2	chr8:143961341-143961391	BJ	skin:	n/a
3	chr8:143961341-143961391	K562	blood:	n/a
4	chr8:143961141-143961191	ovcar-3	ovarian:	n/a
5	chr8:143995000-143995050	NB4	blood:	n/a
6	chr8:143961291-143961341	HRE	kidney:	n/a
7	chr8:143961391-143961441	GM12878	blood:	n/a
8	chr8:143961341-143961391	HIPEpiC	eye:	n/a
9	chr8:143961145-143961195	NT2-D1	testis:	n/a
10	chr8:143961341-143961391	LNCaP	prostate:	n/a
11	chr8:143961145-143961195	NHDF-neo	bronchial:	n/a
12	chr8:143961291-143961341	A549	lung:	n/a
13	chr8:143961141-143961191	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:143961341-143961391	HCF	heart:	n/a
15	chr8:143995000-143995050	GM12878	blood:	n/a
16	chr8:143961291-143961341	HNPCEpiC	eye:	n/a
17	chr8:143961391-143961441	NHDF-neo	bronchial:	n/a
18	chr8:143992652-143992702	HCT-116	colon:	n/a
19	chr8:143961141-143961191	GM12891	blood:	n/a
20	chr8:143961291-143961341	T-47D	breast:	n/a
21	chr8:143992652-143992702	SKMC	muscle:	n/a
22	chr8:143961291-143961341	HEEpiC	esophagus:	n/a
23	chr8:143961391-143961441	HEK293	kidney:	embryo
24	chr8:143961141-143961191	SK-N-SH	brain:	n/a
25	chr8:143961391-143961441	LNCaP	prostate:	n/a
26	chr8:143961391-143961441	NT2-D1	testis:	n/a
27	chr8:143961141-143961191	AG09319	gingival:	n/a
28	chr8:143995000-143995050	SAEC	small airway:	n/a
29	chr8:143961291-143961341	IMR90	lung:	fetal
30	chr8:143961341-143961391	ECC-1	luminal epithelium:	n/a
31	chr8:143961391-143961441	AG09319	gingival:	n/a
32	chr8:143992652-143992702	MCF-7	breast:	n/a
33	chr8:143961141-143961191	GM12878	blood:	n/a
34	chr8:143961291-143961341	Jurkat	blood:	n/a
35	chr8:143992652-143992702	HUVEC	blood vessel:	n/a
36	chr8:143961291-143961341	Caco-2	colon:	n/a
37	chr8:143961141-143961191	CMK	blood:	n/a
38	chr8:143995000-143995050	BE2_C	brain:	n/a
39	chr8:143992652-143992702	AoSMC	blood vessel:	n/a
40	chr8:143961391-143961441	T-47D	breast:	n/a
41	chr8:143961141-143961191	SAEC	small airway:	n/a
42	chr8:143992652-143992702	PrEC	prostate:	n/a
43	chr8:143995000-143995050	Hela-S3	cervix:	n/a
44	chr8:143961145-143961195	AG09319	gingival:	n/a
45	chr8:143961341-143961391	AG04449	skin:	fetal
46	chr8:143995000-143995050	HCT-116	colon:	n/a
47	chr8:143961141-143961191	HAEpiC	amniotic membrane:	n/a
48	chr8:143992652-143992702	NH-A	brain:	n/a
49	chr8:143961341-143961391	H1-hESC	embryonic stem cell:	embryo
50	chr8:143961145-143961195	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:143976851..143979156-chr8:143982564..143985353,2	MCF-7	breast:
2	chr8:143928685..143930379-chr8:143986753..143989580,2	K562	blood:
3	chr8:143982631..143984699-chr8:143987404..143990195,2	K562	blood:
4	chr8:143970505..143972946-chr8:143997611..144000246,2	MCF-7	breast:
5	chr8:143982631..143984699-chr8:143987404..143990195,2	K562	blood:
6	chr8:143955912..143957781-chr8:143987320..143989042,2	MCF-7	breast:
7	chr8:143976851..143979156-chr8:143982564..143985353,2	MCF-7	breast:

Variant related genes	Relation type
CYP11B1	TF binding region
CYP11B1	CpG island
ENSG00000160882	chromatin interactions
ENSG00000179142	chromatin interactions

Extended variants
information (count: 1709 )
Associated
traits (count: 148 )

Variant overlapped rSNPs/rCNVs (count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200952801	chr8:143961099-143961100	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs4534	chr8:143961102-143961103	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs369213890	chr8:143961103-143961104	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs193922538	chr8:143961105-143961106	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs104894069	chr8:143961106-143961107	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs397831740	chr8:143961119-143961120	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs369941128	chr8:143961121-143961122	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs201951316	chr8:143961126-143961127	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs201103987	chr8:143961141-143961142	Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs140274628	chr8:143961142-143961143	Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs144224988	chr8:143961145-143961146	Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs147788769	chr8:143961152-143961153	Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs139569725	chr8:143961153-143961154	Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs61751134	chr8:143961176-143961177	Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs142591816	chr8:143961180-143961181	Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs150983560	chr8:143961186-143961187	Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs6405	chr8:143961201-143961202	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150163594	chr8:143961205-143961206	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200581194	chr8:143961221-143961222	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6389	chr8:143961231-143961232	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373827432	chr8:143961249-143961250	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539054150	chr8:143961255-143961256	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372954252	chr8:143961263-143961264	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs5280	chr8:143961293-143961294	Weak transcription Flanking Active TSS Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs566126580	chr8:143961356-143961357	Weak transcription Flanking Active TSS Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs61751133	chr8:143961379-143961380	Weak transcription Flanking Active TSS Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs555013157	chr8:143961380-143961381	Weak transcription Flanking Active TSS Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs139302686	chr8:143961415-143961416	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs573778824	chr8:143961418-143961419	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs545376395	chr8:143961423-143961424	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs544351684	chr8:143961437-143961438	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs61751131	chr8:143961445-143961446	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs577909770	chr8:143961451-143961452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61751130	chr8:143961454-143961455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575616487	chr8:143961456-143961457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564501320	chr8:143961473-143961474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555641291	chr8:143961498-143961499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376350051	chr8:143961508-143961509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528477303	chr8:143961514-143961515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540744877	chr8:143961544-143961545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377608641	chr8:143961554-143961555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184235880	chr8:143961572-143961573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529466650	chr8:143961579-143961580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374288427	chr8:143961583-143961584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567686896	chr8:143961585-143961586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569340719	chr8:143961604-143961605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533490091	chr8:143961616-143961617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188187504	chr8:143961624-143961625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146403087	chr8:143961627-143961628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201613195	chr8:143961631-143961632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:148)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	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
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	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
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	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
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Gastric cancer	24379144	CNVD
Sezary syndrome	18413736	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20409316	CNVD
Colorectal cancer	16272173	CNVD
Glioma	17123091	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Esophageal squamous carcinoma	17470683	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Astrocytoma	22246337	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	21806811	CNVD
Chylomicronemia	22008945	CNVD
Heart disease	21282601	CNVD
Chordoma	21602918	CNVD
Neuroblastoma	18923191	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	16397240	CNVD
Colorectal cancer	19455253	CNVD
Myxofibrosarcoma	16751306	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
Oral cancer	22144094	CNVD
XY gonadal dysgenesis	20685758	CNVD
Cancer	20581869	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Pancreatic cancer	21811587	CNVD
Prostate cancer	22341455	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:143960800-143961200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:143961000-143961200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
3	chr8:143961000-143961400	Enhancers	Spleen	Spleen
4	chr8:143961200-143961400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
5	chr8:143961200-143969800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:143961400-143961800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr8:143969800-143970400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:143970400-143992600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:143975000-143975600	Enhancers	Duodenum Mucosa	Duodenum
10	chr8:143975800-143976000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:143976000-143977400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:143977400-143977600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:143979000-143979600	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr8:143988000-143989200	Enhancers	HepG2	liver
15	chr8:143991200-143991600	Enhancers	Primary T cells fromperipheralblood	blood
16	chr8:143991200-143991600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr8:143991200-143992200	Enhancers	Spleen	Spleen
18	chr8:143991400-143992000	Enhancers	Primary B cells from peripheral blood	blood
19	chr8:143992200-143993200	Weak transcription	Spleen	Spleen
20	chr8:143992600-143993400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr8:143993200-143993400	Enhancers	Spleen	Spleen
22	chr8:143993400-143993600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr8:143993400-143993600	Genic enhancers	Spleen	Spleen
24	chr8:143993400-143993800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:143993600-143995000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr8:143993600-143995200	Weak transcription	Spleen	Spleen
27	chr8:143993800-143994200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr8:143994200-144003200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:143994400-143994600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr8:143994800-143995400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr8:143995000-143995400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr8:143995200-143996000	Enhancers	Spleen	Spleen
33	chr8:143995400-143995600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr8:143996000-144003000	Weak transcription	Spleen	Spleen

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