Variant report

Variant	nsv831427
Chromosome Location	chr8:113494319-113699264
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	chr8:113500282-113500373	K562	blood:	n/a	n/a
2	BCL3	chr8:113623801-113624046	GM12878	blood:	n/a	n/a
3	CEBPB	chr8:113584277-113584402	H1-hESC	embryonic stem cell:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
4	CEBPB	chr8:113675869-113676172	K562	blood:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
5	CEBPB	chr8:113584132-113584520	A549	lung:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
6	CEBPB	chr8:113682533-113683041	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr8:113675862-113676155	H1-hESC	embryonic stem cell:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
8	CEBPB	chr8:113513141-113513369	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr8:113584151-113584545	Hela-S3	cervix:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
10	CEBPB	chr8:113584252-113584508	A549	lung:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
11	CEBPB	chr8:113675839-113676178	MCF-7	breast:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
12	CEBPB	chr8:113584242-113584491	K562	blood:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
13	CEBPB	chr8:113584173-113584544	HepG2	liver:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
14	CEBPB	chr8:113574808-113574989	A549	lung:	n/a	chr8:113574860-113574871 chr8:113574860-113574873 chr8:113574860-113574873
15	CEBPB	chr8:113513135-113513454	MCF-7	breast:	n/a	n/a
16	CEBPB	chr8:113574810-113574943	H1-hESC	embryonic stem cell:	n/a	chr8:113574860-113574871 chr8:113574860-113574873 chr8:113574860-113574873
17	CEBPB	chr8:113675831-113676188	HepG2	liver:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
18	CEBPB	chr8:113695353-113695608	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:113543052-113543379	HepG2	liver:	n/a	chr8:113543224-113543235
20	CEBPB	chr8:113584175-113584533	IMR90	lung:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
21	CEBPB	chr8:113675853-113676190	A549	lung:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
22	CEBPB	chr8:113680956-113681228	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:113628682-113629030	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr8:113675826-113676181	IMR90	lung:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
25	CEBPB	chr8:113675839-113676180	Hela-S3	cervix:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
26	CTCF	chr8:113649045-113649108	MCF-7	breast:	n/a	n/a
27	CTCF	chr8:113501365-113501423	LNCaP	prostate:	n/a	n/a
28	CTCF	chr8:113503788-113503843	GM13976	blood:	n/a	n/a
29	CTCF	chr8:113697658-113697706	GM10248	blood:	n/a	n/a
30	CTCF	chr8:113634580-113634730	MCF-7	breast:	n/a	n/a
31	E2F4	chr8:113672535-113672733	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr8:113696988-113697270	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr8:113520520-113520674	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr8:113509533-113509730	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr8:113601616-113601796	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr8:113577530-113577661	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr8:113682728-113683040	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr8:113566230-113566398	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr8:113644284-113644571	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr8:113686741-113686999	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr8:113680266-113680439	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr8:113599633-113599785	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr8:113685558-113685640	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr8:113623744-113624050	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F6	chr8:113564490-113564847	H1-hESC	embryonic stem cell:	n/a	n/a
46	E2F6	chr8:113564522-113564753	H1-hESC	embryonic stem cell:	n/a	n/a
47	EP300	chr8:113690751-113690802	K562	blood:	n/a	n/a
48	EP300	chr8:113523133-113523272	K562	blood:	n/a	n/a
49	EP300	chr8:113660100-113660633	MCF-7	breast:	n/a	n/a
50	EP300	chr8:113654305-113654316	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:113655561-113655611	Jurkat	blood:	n/a
2	chr8:113656015-113656065	SK-N-SH	brain:	n/a
3	chr8:113655561-113655611	HCPEpiC	choroid plexus:	n/a
4	chr8:113655436-113655486	SK-N-SH	brain:	n/a
5	chr8:113656015-113656065	CMK	blood:	n/a
6	chr8:113655561-113655611	NHDF-neo	bronchial:	n/a
7	chr8:113655561-113655611	GM12892	blood:	n/a
8	chr8:113655561-113655611	AG04450	lung:	fetal
9	chr8:113655561-113655611	HCT-116	colon:	n/a
10	chr8:113656015-113656065	GM06990	blood:	n/a
11	chr8:113655436-113655486	AG04449	skin:	fetal
12	chr8:113656015-113656065	HCPEpiC	choroid plexus:	n/a
13	chr8:113655561-113655611	ProgFib	skin:	n/a
14	chr8:113655436-113655486	HEEpiC	esophagus:	n/a
15	chr8:113656015-113656065	PFSK-1	brain:	n/a
16	chr8:113655561-113655611	GM12878	blood:	n/a
17	chr8:113655436-113655486	HEK293	kidney:	embryo
18	chr8:113656015-113656065	HNPCEpiC	eye:	n/a
19	chr8:113656015-113656065	MCF-7	breast:	n/a
20	chr8:113655561-113655611	BJ	skin:	n/a
21	chr8:113655561-113655611	IMR90	lung:	fetal
22	chr8:113655561-113655611	HEEpiC	esophagus:	n/a
23	chr8:113655436-113655486	HPAEpiC	pulmonary alveolar:	n/a
24	chr8:113655436-113655486	HepG2	liver:	n/a
25	chr8:113656015-113656065	K562	blood:	n/a
26	chr8:113655436-113655486	MCF-7	breast:	n/a
27	chr8:113655436-113655486	Jurkat	blood:	n/a
28	chr8:113656015-113656065	GM12891	blood:	n/a
29	chr8:113655561-113655611	K562	blood:	n/a
30	chr8:113655561-113655611	PrEC	prostate:	n/a
31	chr8:113655436-113655486	AG09319	gingival:	n/a
32	chr8:113655436-113655486	HCPEpiC	choroid plexus:	n/a
33	chr8:113656015-113656065	HEEpiC	esophagus:	n/a
34	chr8:113656015-113656065	HCM	heart:	n/a
35	chr8:113655436-113655486	CMK	blood:	n/a
36	chr8:113655436-113655486	PrEC	prostate:	n/a
37	chr8:113656015-113656065	HCT-116	colon:	n/a
38	chr8:113656015-113656065	Hepatocyte	liver:	n/a
39	chr8:113656015-113656065	AG10803	skin:	n/a
40	chr8:113655561-113655611	AoSMC	blood vessel:	n/a
41	chr8:113656015-113656065	AG09319	gingival:	n/a
42	chr8:113655436-113655486	GM12892	blood:	n/a
43	chr8:113655561-113655611	HRCEpiC	kidney:	n/a
44	chr8:113656015-113656065	A549	lung:	n/a
45	chr8:113655561-113655611	SKMC	muscle:	n/a
46	chr8:113655561-113655611	HMEC	breast:	n/a
47	chr8:113655561-113655611	GM06990	blood:	n/a
48	chr8:113655561-113655611	MCF10A-Er-Src	breast:	n/a
49	chr8:113656015-113656065	PrEC	prostate:	n/a
50	chr8:113656015-113656065	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:113623376..113625406-chr8:113626015..113627569,2	MCF-7	breast:
2	chr8:113623376..113625406-chr8:113626015..113627569,2	MCF-7	breast:
3	chr20:18661388..18664062-chr8:113586254..113588798,2	MCF-7	breast:
4	chr8:113648317..113650428-chr8:113651221..113653011,2	MCF-7	breast:
5	chr8:112878252..112879995-chr8:113601916..113604196,2	MCF-7	breast:
6	chr8:113656932..113658484-chr8:113659367..113661819,2	K562	blood:
7	chr8:113495952..113497684-chr8:113532113..113534940,2	MCF-7	breast:
8	chr8:113648317..113650428-chr8:113651221..113653011,2	MCF-7	breast:
9	chr8:113536029..113539003-chr8:113540588..113542968,2	MCF-7	breast:
10	chr8:113659187..113660730-chr8:113666931..113668583,2	MCF-7	breast:
11	chr11:85195583..85198227-chr8:113682885..113684772,2	MCF-7	breast:
12	chr8:113656932..113658484-chr8:113659367..113661819,2	K562	blood:
13	chr8:113659187..113660730-chr8:113666931..113668583,2	MCF-7	breast:
14	chr8:113536029..113539003-chr8:113540588..113542968,2	MCF-7	breast:
15	chr6:30778063..30780102-chr8:113652986..113654698,2	MCF-7	breast:
16	chr8:113495952..113497684-chr8:113532113..113534940,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-67H2.1.1-6	chr8:113551118-113551546	NONHSAT128340

miRNA name	Chromosome Location	mirBase accession
hsa-miR-2053	chr8:113655782-113655804	MIMAT0009978

Variant related genes	Relation type
ENSG00000238656	TF binding region
RPL30P16	TF binding region
MIR2053	TF binding region
ENSG00000238656	CpG island
RPL30P16	CpG island
MIR2053	CpG island

Extended variants
information (count: 7045 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:7045 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537372045	chr8:113494340-113494341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190052213	chr8:113494361-113494362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541196286	chr8:113494390-113494391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564286298	chr8:113494391-113494392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558844326	chr8:113494399-113494400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533216869	chr8:113494433-113494434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576988438	chr8:113494442-113494443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550097810	chr8:113494462-113494463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570006752	chr8:113494506-113494507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528868891	chr8:113494512-113494513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376918796	chr8:113494567-113494568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147845813	chr8:113494594-113494595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565611568	chr8:113494612-113494613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141374563	chr8:113494678-113494679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541533776	chr8:113494697-113494698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570713360	chr8:113494718-113494719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539689541	chr8:113494756-113494757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556428952	chr8:113494760-113494761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200893103	chr8:113494778-113494779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201582650	chr8:113494860-113494861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201758577	chr8:113494919-113494920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11995388	chr8:113494927-113494928	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs555009564	chr8:113494930-113494931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146982288	chr8:113494934-113494935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555749462	chr8:113494935-113494936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572411493	chr8:113494988-113494989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183033751	chr8:113494990-113494991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138064755	chr8:113495003-113495004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554294086	chr8:113495013-113495014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543678233	chr8:113495045-113495046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142071882	chr8:113495053-113495054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574374194	chr8:113495085-113495086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200088698	chr8:113495146-113495147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529209871	chr8:113495152-113495153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553004509	chr8:113495158-113495159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11784490	chr8:113495182-113495183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548666443	chr8:113495184-113495185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368276703	chr8:113495256-113495257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150104587	chr8:113495261-113495262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574921637	chr8:113495282-113495283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188370072	chr8:113495288-113495289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7832966	chr8:113495325-113495326	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs7833084	chr8:113495333-113495334	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs539629631	chr8:113495388-113495389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367996907	chr8:113495458-113495459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs193019421	chr8:113495463-113495464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536158944	chr8:113495470-113495471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183924993	chr8:113495525-113495526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572403627	chr8:113495535-113495536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1020597	chr8:113495545-113495546	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:102)

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
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
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
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
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Schizophrenia	20967226	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113484200-113496200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:113492400-113496000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:113495600-113496200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:113496000-113496200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:113496200-113496400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:113507400-113507800	Enhancers	Fetal Brain Male	brain
7	chr8:113512600-113513000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr8:113512600-113513200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr8:113512600-113513200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr8:113512800-113513200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr8:113512800-113513200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:113512800-113513400	Enhancers	H1 Cell Line	embryonic stem cell
13	chr8:113512800-113513400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr8:113512800-113513400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr8:113513000-113513400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:113513000-113513400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:113513200-113513400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:113513400-113520400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:113513400-113520400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:113519800-113520200	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr8:113520000-113520600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:113520000-113520600	Active TSS	A549	lung
23	chr8:113520200-113520400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
24	chr8:113520200-113520800	Active TSS	Duodenum Mucosa	Duodenum
25	chr8:113520200-113520800	Active TSS	Rectal Mucosa Donor 29	rectum
26	chr8:113520200-113521000	Enhancers	Stomach Mucosa	stomach
27	chr8:113520200-113521200	Enhancers	NHEK	skin
28	chr8:113520400-113520600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:113520400-113520800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr8:113520400-113520800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr8:113520400-113520800	Active TSS	Brain Anterior Caudate	brain
32	chr8:113520400-113520800	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr8:113520400-113521000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:113520600-113520800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:113520600-113520800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr8:113520800-113521000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:113520800-113521000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:113520800-113524000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr8:113521000-113522000	Weak transcription	Stomach Mucosa	stomach
40	chr8:113522000-113522200	Enhancers	Stomach Mucosa	stomach
41	chr8:113524000-113525200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:113525200-113542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr8:113534800-113536800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr8:113535000-113535800	Enhancers	Fetal Lung	lung
45	chr8:113536000-113536400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr8:113540600-113543000	Weak transcription	NHEK	skin
47	chr8:113541000-113541200	Enhancers	Brain Germinal Matrix	brain
48	chr8:113541400-113542400	Weak transcription	Brain Germinal Matrix	brain
49	chr8:113541600-113541800	Weak transcription	Fetal Lung	lung
50	chr8:113541800-113543400	Enhancers	Fetal Lung	lung

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