Variant report

Variant	nsv523000
Chromosome Location	chr8:132304508-132329300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:53)
CpG islands
(count:123)
Chromatin interactive
region (count:0)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:53 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:132312981-132313310	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr8:132308012-132308313	HepG2	liver:	n/a	chr8:132308136-132308147
3	CEBPB	chr8:132308016-132308282	IMR90	lung:	n/a	chr8:132308136-132308147
4	CEBPB	chr8:132308001-132308313	A549	lung:	n/a	chr8:132308136-132308147
5	CEBPB	chr8:132308078-132308278	K562	blood:	n/a	chr8:132308136-132308147
6	CTCF	chr8:132312532-132312569	Fibrobl	skin:	n/a	n/a
7	CTCF	chr8:132323352-132323437	GM13976	blood:	n/a	n/a
8	E2F4	chr8:132318964-132319081	MCF10A-Er-Src	breast:	n/a	n/a
9	E2F4	chr8:132307589-132307772	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr8:132307668-132307833	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr8:132308809-132309036	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr8:132307668-132308009	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr8:132307677-132307845	MCF10A-Er-Src	breast:	n/a	n/a
14	FOXA2	chr8:132326977-132327368	A549	lung:	n/a	n/a
15	FOXA2	chr8:132327115-132327431	A549	lung:	n/a	n/a
16	GATA3	chr8:132306923-132307096	SH-SY5Y	brain:	n/a	n/a
17	MAX	chr8:132313011-132313327	H1-hESC	embryonic stem cell:	n/a	n/a
18	MAZ	chr8:132328976-132328995	HepG2	liver:	n/a	n/a
19	MXI1	chr8:132315076-132315100	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr8:132322290-132322445	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr8:132327765-132327938	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr8:132304997-132304999	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr8:132319267-132319291	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr8:132320495-132321126	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr8:132312470-132312630	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr8:132322385-132323097	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr8:132328119-132328227	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr8:132311515-132311710	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr8:132328399-132328638	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr8:132324542-132324709	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr8:132322607-132322973	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr8:132327988-132328280	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr8:132327684-132332209	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr8:132328659-132328993	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr8:132307803-132307935	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr8:132322676-132322908	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr8:132328100-132328114	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr8:132324109-132324268	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr8:132318929-132318987	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr8:132312481-132312594	A549	lung:	n/a	n/a
41	POLR2A	chr8:132328659-132329162	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr8:132317805-132317831	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr8:132328027-132328255	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr8:132328690-132328870	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr8:132310980-132311000	MCF10A-Er-Src	breast:	n/a	n/a
46	REST	chr8:132312441-132312684	HCT-116	colon:	n/a	n/a
47	STAT3	chr8:132328275-132328920	MCF10A-Er-Src	breast:	n/a	n/a
48	STAT3	chr8:132307801-132307830	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT3	chr8:132317753-132317803	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr8:132307688-132307882	MCF10A-Er-Src	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:132313141-132313191	HRCEpiC	kidney:	n/a
2	chr8:132313141-132313191	HRCEpiC	kidney:	n/a
3	chr8:132313141-132313191	A549	lung:	n/a
4	chr8:132321917-132321967	A549	lung:	n/a
5	chr8:132321917-132321967	BE2_C	brain:	n/a
6	chr8:132313141-132313191	SKMC	muscle:	n/a
7	chr8:132321917-132321967	HRPEpiC	eye:	n/a
8	chr8:132321917-132321967	GM12892	blood:	n/a
9	chr8:132313141-132313191	BJ	skin:	n/a
10	chr8:132313141-132313191	Hela-S3	cervix:	n/a
11	chr8:132321917-132321967	HEEpiC	esophagus:	n/a
12	chr8:132313141-132313191	AG09319	gingival:	n/a
13	chr8:132321917-132321967	GM19239	blood:	n/a
14	chr8:132313141-132313191	GM12878	blood:	n/a
15	chr8:132321917-132321967	H1-hESC	embryonic stem cell:	embryo
16	chr8:132321917-132321967	HAEpiC	amniotic membrane:	n/a
17	chr8:132313141-132313191	NHDF-neo	bronchial:	n/a
18	chr8:132313141-132313191	AoSMC	blood vessel:	n/a
19	chr8:132313141-132313191	SK-N-SH_RA	brain:	n/a
20	chr8:132321917-132321967	HRCEpiC	kidney:	n/a
21	chr8:132313141-132313191	MCF-7	breast:	n/a
22	chr8:132313141-132313191	PrEC	prostate:	n/a
23	chr8:132313141-132313191	PFSK-1	brain:	n/a
24	chr8:132321917-132321967	NB4	blood:	n/a
25	chr8:132313141-132313191	ProgFib	skin:	n/a
26	chr8:132321917-132321967	PANC-1	pancreas:	n/a
27	chr8:132321917-132321967	AoSMC	blood vessel:	n/a
28	chr8:132321917-132321967	AG04450	lung:	fetal
29	chr8:132313141-132313191	NHBE	bronchial:	n/a
30	chr8:132313141-132313191	HEEpiC	esophagus:	n/a
31	chr8:132321917-132321967	U87	brain:	n/a
32	chr8:132321917-132321967	HCM	heart:	n/a
33	chr8:132321917-132321967	BJ	skin:	n/a
34	chr8:132321917-132321967	Hela-S3	cervix:	n/a
35	chr8:132321917-132321967	HRE	kidney:	n/a
36	chr8:132321917-132321967	HCT-116	colon:	n/a
37	chr8:132321917-132321967	ProgFib	skin:	n/a
38	chr8:132321917-132321967	NH-A	brain:	n/a
39	chr8:132313141-132313191	HRPEpiC	eye:	n/a
40	chr8:132313141-132313191	HCPEpiC	choroid plexus:	n/a
41	chr8:132321917-132321967	HepG2	liver:	n/a
42	chr8:132313141-132313191	IMR90	lung:	fetal
43	chr8:132313141-132313191	AG09309	skin:	n/a
44	chr8:132313141-132313191	K562	blood:	n/a
45	chr8:132313141-132313191	HCM	heart:	n/a
46	chr8:132321917-132321967	HEK293	kidney:	embryo
47	chr8:132313141-132313191	SAEC	small airway:	n/a
48	chr8:132313141-132313191	PANC-1	pancreas:	n/a
49	chr8:132313141-132313191	Jurkat	blood:	n/a
50	chr8:132321917-132321967	RPTEC	kidney:	n/a

No data

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFR3A-1	chr8:132320792-132320918	ENSG00000253507
2	lnc-EFR3A-1	chr8:132322719-132322959	ENSG00000253507
3	lnc-EFR3A-1	chr8:132327256-132328130	NONHSAT129174
4	lnc-EFR3A-1	chr8:132320792-132320918	ENSG00000253507
5	lnc-EFR3A-1	chr8:132324624-132325013	NONHSAT129174
6	lnc-EFR3A-1	chr8:132327084-132327225	NONHSAT129174
7	lnc-EFR3A-1	chr8:132328007-132328130	ENSG00000253507
8	lnc-EFR3A-1	chr8:132320762-132320918	NONHSAT129170
9	lnc-EFR3A-1	chr8:132328007-132328130	ENSG00000253507
10	lnc-EFR3A-1	chr8:132328007-132328130	ENSG00000253507
11	lnc-EFR3A-1	chr8:132324803-132324995	ENSG00000253507
12	lnc-EFR3A-1	chr8:132322800-132322959	ENSG00000253507
13	lnc-EFR3A-1	chr8:132324803-132324976	ENSG00000253507
14	lnc-EFR3A-1	chr8:132324803-132324995	ENSG00000253507
15	lnc-EFR3A-1	chr8:132322800-132323052	NONHSAT129170
16	lnc-EFR3A-1	chr8:132322800-132322959	ENSG00000253507

No data

Variant related genes	Relation type
ENSG00000253507	TF binding region
ENSG00000253507	CpG island

Extended variants
information (count: 1019 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:1019 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10102742	chr8:132304508-132304509	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76555409	chr8:132304595-132304596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144352632	chr8:132304643-132304644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143283693	chr8:132304646-132304647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs67989847	chr8:132304647-132304648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10088081	chr8:132304648-132304649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565350757	chr8:132304662-132304663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375977064	chr8:132304666-132304667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11784942	chr8:132304668-132304669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190354552	chr8:132304686-132304687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369184741	chr8:132304715-132304716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs57207971	chr8:132304752-132304753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138137378	chr8:132304810-132304811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548206275	chr8:132304838-132304839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76909711	chr8:132304933-132304934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72716498	chr8:132304942-132304943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551877886	chr8:132304954-132304955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57417387	chr8:132305045-132305046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183203279	chr8:132305071-132305072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142619160	chr8:132305109-132305110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561083780	chr8:132305134-132305135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113411979	chr8:132305167-132305168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573193072	chr8:132305174-132305175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574724575	chr8:132305195-132305196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535378059	chr8:132305198-132305199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373774880	chr8:132305202-132305203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144880805	chr8:132305216-132305217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540316887	chr8:132305340-132305341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187839261	chr8:132305394-132305395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532688690	chr8:132305442-132305443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577363707	chr8:132305471-132305472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544864693	chr8:132305487-132305488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562927913	chr8:132305494-132305495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530457605	chr8:132305501-132305502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551175218	chr8:132305557-132305558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376233670	chr8:132305559-132305560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548577201	chr8:132305564-132305565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560812408	chr8:132305604-132305605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569320672	chr8:132305633-132305634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78615193	chr8:132305661-132305662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563100759	chr8:132305663-132305664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551717175	chr8:132305666-132305667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138612827	chr8:132305667-132305668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552728871	chr8:132305673-132305674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531649957	chr8:132305699-132305700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149293584	chr8:132305705-132305706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572638189	chr8:132305713-132305714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535192630	chr8:132305741-132305742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536492939	chr8:132305761-132305762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368764426	chr8:132305766-132305767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

Disease	PMID	Source
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
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
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
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
Endometrioid adenocarcinoma	16974079	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
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	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
Malignant melanoma	17260012	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastric cancer	16891809	CNVD
Colorectal cancer	19455253	CNVD
Pregnancies with abnormal ultrasound findings	21110858	CNVD
Breast cancer	19181860	CNVD
Brain cancer	19584924	CNVD
Medulloblastoma	19584924	CNVD
Follicular lymphoma	17699855	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:132302400-132307600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:132303200-132306200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:132303400-132307600	Weak transcription	HMEC	breast
4	chr8:132303600-132307800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:132304400-132305600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:132305800-132306000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:132306200-132306400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:132306400-132306600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:132307600-132308000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr8:132307600-132308000	Enhancers	HMEC	breast
11	chr8:132307600-132309000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:132307800-132308400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:132311600-132312800	Enhancers	Fetal Intestine Large	intestine
14	chr8:132312400-132312600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:132312600-132312800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:132312600-132313600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
17	chr8:132312800-132313000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr8:132312800-132313200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
19	chr8:132313000-132313800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr8:132313000-132313800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr8:132313200-132313400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
22	chr8:132313200-132313600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
23	chr8:132313200-132313600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr8:132313200-132313600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr8:132313400-132313600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
26	chr8:132313600-132313800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
27	chr8:132313800-132314000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
28	chr8:132315600-132321600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:132319200-132320000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr8:132319400-132319600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr8:132320000-132320200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr8:132320200-132321200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:132320200-132321200	Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr8:132320800-132321000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
35	chr8:132320800-132321200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
36	chr8:132320800-132321200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
37	chr8:132320800-132321600	Active TSS	H1 Cell Line	embryonic stem cell
38	chr8:132320800-132321600	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr8:132320800-132321600	Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr8:132320800-132321800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr8:132321000-132326400	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr8:132321200-132321400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr8:132321200-132321400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr8:132321200-132321600	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr8:132321200-132322000	Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr8:132321200-132325600	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
47	chr8:132321400-132321800	Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr8:132321400-132322000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr8:132321400-132325400	Active TSS	H9 Cell Line	embryonic stem cell
50	chr8:132321600-132321800	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell

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