Variant report

Variant	nsv547987
Chromosome Location	chr1:158664972-158720188
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:610)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:158704604-158704729	K562	blood:	n/a	n/a
2	ARID3A	chr1:158698592-158698924	K562	blood:	n/a	n/a
3	ARID3A	chr1:158709982-158710193	K562	blood:	n/a	n/a
4	ARID3A	chr1:158702324-158702669	K562	blood:	n/a	n/a
5	ARID3A	chr1:158699545-158699797	K562	blood:	n/a	n/a
6	ATF2	chr1:158685985-158686572	GM12878	blood:	n/a	n/a
7	ATF2	chr1:158685997-158686610	GM12878	blood:	n/a	n/a
8	BACH1	chr1:158701798-158702048	K562	blood:	n/a	n/a
9	BATF	chr1:158686205-158686468	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:158686138-158686476	GM12878	blood:	n/a	chr1:158686264-158686273 chr1:158686265-158686274
11	BCLAF1	chr1:158686191-158686569	GM12878	blood:	n/a	chr1:158686264-158686273 chr1:158686265-158686274
12	BHLHE40	chr1:158701588-158702091	K562	blood:	n/a	n/a
13	CEBPB	chr1:158719042-158719256	HepG2	liver:	n/a	chr1:158719183-158719196 chr1:158719183-158719194
14	CEBPB	chr1:158705115-158705187	K562	blood:	n/a	n/a
15	CEBPB	chr1:158689483-158689802	K562	blood:	n/a	n/a
16	CEBPB	chr1:158680686-158680988	A549	lung:	n/a	chr1:158680816-158680827
17	CEBPB	chr1:158680689-158680944	IMR90	lung:	n/a	chr1:158680816-158680827
18	CEBPB	chr1:158711092-158711357	K562	blood:	n/a	n/a
19	CEBPB	chr1:158680660-158680979	HepG2	liver:	n/a	chr1:158680816-158680827
20	CEBPB	chr1:158680693-158680923	K562	blood:	n/a	chr1:158680816-158680827
21	CEBPB	chr1:158719103-158719306	A549	lung:	n/a	chr1:158719183-158719196 chr1:158719183-158719194
22	CEBPD	chr1:158702247-158702768	K562	blood:	n/a	n/a
23	CEBPD	chr1:158702210-158702773	K562	blood:	n/a	n/a
24	CHD2	chr1:158707497-158707550	K562	blood:	n/a	n/a
25	CTCF	chr1:158669880-158670030	GM12865	blood:	n/a	n/a
26	CTCF	chr1:158703490-158703560	GM20000	blood:	n/a	n/a
27	CTCF	chr1:158684800-158684950	NHEK	skin:	n/a	n/a
28	CTCF	chr1:158684720-158684870	GM12875	blood:	n/a	n/a
29	CTCF	chr1:158684600-158684750	K562	blood:	n/a	n/a
30	CTCF	chr1:158684680-158684830	GM12873	blood:	n/a	n/a
31	CTCF	chr1:158684660-158684810	GM12872	blood:	n/a	n/a
32	CTCF	chr1:158684660-158684810	GM12873	blood:	n/a	n/a
33	CTCF	chr1:158669730-158669755	ProgFib	skin:	n/a	n/a
34	CUX1	chr1:158695399-158695430	GM12878	blood:	n/a	n/a
35	E2F4	chr1:158711498-158711698	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr1:158699343-158699536	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr1:158686002-158686276	MCF10A-Er-Src	breast:	n/a	n/a
38	EBF1	chr1:158703222-158703483	GM12878	blood:	n/a	chr1:158703323-158703334
39	EBF1	chr1:158686165-158686470	GM12878	blood:	n/a	n/a
40	EP300	chr1:158666572-158666589	GM12878	blood:	n/a	n/a
41	EP300	chr1:158686114-158686554	GM12878	blood:	n/a	chr1:158686265-158686274 chr1:158686489-158686496
42	EP300	chr1:158669238-158669278	K562	blood:	n/a	n/a
43	EP300	chr1:158701733-158702739	K562	blood:	n/a	n/a
44	EP300	chr1:158686175-158686557	GM12878	blood:	n/a	chr1:158686489-158686496 chr1:158686265-158686274
45	EP300	chr1:158699994-158700054	GM12878	blood:	n/a	n/a
46	EP300	chr1:158686199-158686421	GM12878	blood:	n/a	chr1:158686265-158686274
47	EP300	chr1:158708315-158708350	K562	blood:	n/a	n/a
48	EP300	chr1:158698444-158698971	K562	blood:	n/a	n/a
49	FOS	chr1:158711179-158711378	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:158687170-158687297	MCF10A-Er-Src	breast:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158671873-158671923	MCF-7	breast:	n/a
2	chr1:158670397-158670447	HCM	heart:	n/a
3	chr1:158670397-158670447	HepG2	liver:	n/a
4	chr1:158670124-158670174	BJ	skin:	n/a
5	chr1:158688804-158688854	HUVEC	blood vessel:	n/a
6	chr1:158671873-158671923	RPTEC	kidney:	n/a
7	chr1:158687431-158687481	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:158688926-158688976	NH-A	brain:	n/a
9	chr1:158688804-158688854	PFSK-1	brain:	n/a
10	chr1:158688926-158688976	GM19239	blood:	n/a
11	chr1:158689263-158689313	NHDF-neo	bronchial:	n/a
12	chr1:158688926-158688976	BJ	skin:	n/a
13	chr1:158689141-158689191	SK-N-SH	brain:	n/a
14	chr1:158670124-158670174	HUVEC	blood vessel:	n/a
15	chr1:158670124-158670174	HEEpiC	esophagus:	n/a
16	chr1:158687431-158687481	HCM	heart:	n/a
17	chr1:158689263-158689313	U87	brain:	n/a
18	chr1:158670124-158670174	SKMC	muscle:	n/a
19	chr1:158670397-158670447	BE2_C	brain:	n/a
20	chr1:158671873-158671923	PFSK-1	brain:	n/a
21	chr1:158688926-158688976	HCT-116	colon:	n/a
22	chr1:158689263-158689313	Jurkat	blood:	n/a
23	chr1:158671873-158671923	PANC-1	pancreas:	n/a
24	chr1:158688804-158688854	Caco-2	colon:	n/a
25	chr1:158688804-158688854	HEEpiC	esophagus:	n/a
26	chr1:158687431-158687481	HRCEpiC	kidney:	n/a
27	chr1:158687431-158687481	NT2-D1	testis:	n/a
28	chr1:158689263-158689313	MCF10A-Er-Src	breast:	n/a
29	chr1:158689141-158689191	GM12878	blood:	n/a
30	chr1:158670397-158670447	GM19239	blood:	n/a
31	chr1:158688804-158688854	ProgFib	skin:	n/a
32	chr1:158689263-158689313	NB4	blood:	n/a
33	chr1:158671873-158671923	K562	blood:	n/a
34	chr1:158670124-158670174	HNPCEpiC	eye:	n/a
35	chr1:158688804-158688854	AG04449	skin:	fetal
36	chr1:158670397-158670447	Hela-S3	cervix:	n/a
37	chr1:158688775-158688825	MCF-7	breast:	n/a
38	chr1:158689263-158689313	AG09319	gingival:	n/a
39	chr1:158687431-158687481	H1-hESC	embryonic stem cell:	embryo
40	chr1:158671873-158671923	NB4	blood:	n/a
41	chr1:158687431-158687481	HCF	heart:	n/a
42	chr1:158671873-158671923	NHDF-neo	bronchial:	n/a
43	chr1:158687431-158687481	HUVEC	blood vessel:	n/a
44	chr1:158689141-158689191	HMEC	breast:	n/a
45	chr1:158689141-158689191	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:158670617-158670667	MCF-7	breast:	n/a
47	chr1:158671873-158671923	HEEpiC	esophagus:	n/a
48	chr1:158687431-158687481	HRE	kidney:	n/a
49	chr1:158689263-158689313	A549	lung:	n/a
50	chr1:158688804-158688854	HRPEpiC	eye:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:158676105..158677828-chr1:158684515..158686089,2	K562	blood:
2	chr1:158669887..158672800-chr1:158674715..158677591,2	K562	blood:
3	chr1:158697116..158699497-chr1:158702619..158704927,2	K562	blood:
4	chr1:158696982..158701883-chr1:158702210..158705771,7	K562	blood:
5	chr1:158715265..158717778-chr1:158778694..158781362,2	K562	blood:
6	chr1:158699118..158701949-chr1:158709331..158711984,2	K562	blood:
7	chr1:158659297..158661841-chr1:158675200..158677714,2	K562	blood:
8	chr1:158701358..158703864-chr1:158711036..158713684,2	K562	blood:
9	chr1:158697116..158699497-chr1:158702619..158704927,2	K562	blood:
10	chr1:158691383..158694379-chr1:158696049..158697811,2	K562	blood:
11	chr1:158691573..158694598-chr1:158696049..158698060,3	K562	blood:
12	chr1:158661667..158663696-chr1:158666950..158669041,2	K562	blood:
13	chr1:158653549..158656527-chr1:158701529..158703994,2	K562	blood:
14	chr1:158696982..158701883-chr1:158702210..158705771,7	K562	blood:
15	chr1:158659639..158662606-chr1:158667652..158670080,3	K562	blood:
16	chr1:158711568..158713375-chr1:158713499..158715477,2	K562	blood:
17	chr1:158674913..158677154-chr1:158686436..158687990,2	K562	blood:
18	chr1:158649920..158652819-chr1:158694905..158696838,2	K562	blood:
19	chr1:158701755..158705583-chr1:158706296..158709041,3	K562	blood:
20	chr1:158701755..158705583-chr1:158706296..158709041,3	K562	blood:
21	chr1:158702009..158703945-chr1:158717255..158718973,2	K562	blood:
22	chr1:158699118..158701949-chr1:158709331..158711984,2	K562	blood:
23	chr1:158704822..158706927-chr1:158777581..158780196,2	K562	blood:
24	chr1:158676105..158677828-chr1:158684515..158686089,2	K562	blood:
25	chr1:158691573..158694598-chr1:158696049..158698060,3	K562	blood:
26	chr1:158702009..158703945-chr1:158717255..158718973,2	K562	blood:
27	chr1:158691383..158694379-chr1:158696049..158697811,2	K562	blood:
28	chr1:158684463..158686914-chr1:158687743..158690259,2	K562	blood:

No data

Variant related genes	Relation type
OR6K6	TF binding region
OR6K4P	TF binding region
OR6K5P	TF binding region
OR6K3	TF binding region
OR6K1P	TF binding region
OR6K2	TF binding region
OR6K6	CpG island
OR6K4P	CpG island
OR6K5P	CpG island
OR6K3	CpG island
OR6K1P	CpG island
OR6K2	CpG island
ENSG00000163554	chromatin interactions
ENSG00000203757	chromatin interactions
ENSG00000180409	chromatin interactions
ENSG00000226949	chromatin interactions
ENSG00000196171	chromatin interactions

Extended variants
information (count: 1577 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1577 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12023371	chr1:158664972-158664973	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112046208	chr1:158664973-158664974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539176932	chr1:158664981-158664982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369795949	chr1:158664989-158664990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557418524	chr1:158665000-158665001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188220287	chr1:158665010-158665011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138567732	chr1:158665014-158665015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577322798	chr1:158665073-158665074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs703126	chr1:158665117-158665118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs530565928	chr1:158665126-158665127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549939817	chr1:158665165-158665166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568350817	chr1:158665182-158665183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563198097	chr1:158665183-158665184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529511236	chr1:158665191-158665192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539821999	chr1:158665227-158665228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576708550	chr1:158665232-158665233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548092041	chr1:158665238-158665239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565888687	chr1:158665246-158665247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35490186	chr1:158665255-158665256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539831215	chr1:158665272-158665273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551527278	chr1:158665276-158665277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570162107	chr1:158665277-158665278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542498651	chr1:158665288-158665289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537572695	chr1:158665304-158665305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555587986	chr1:158665308-158665309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181183582	chr1:158665331-158665332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562177593	chr1:158665333-158665334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573900776	chr1:158665356-158665357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534565346	chr1:158665360-158665361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562019645	chr1:158665378-158665379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527864377	chr1:158665379-158665380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374815352	chr1:158665391-158665392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577898856	chr1:158665431-158665432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544985354	chr1:158665461-158665462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562972123	chr1:158665498-158665499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536906284	chr1:158665506-158665507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540604609	chr1:158665520-158665521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1235797	chr1:158665523-158665524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs60294930	chr1:158665525-158665526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12757564	chr1:158665526-158665527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368583709	chr1:158665529-158665530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375586693	chr1:158665551-158665552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561918143	chr1:158665631-158665632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369266983	chr1:158665635-158665636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529493957	chr1:158665649-158665650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200978404	chr1:158665693-158665694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546310642	chr1:158665714-158665715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573813661	chr1:158665737-158665738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115176593	chr1:158665761-158665762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs326000	chr1:158665815-158665816	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	21045282	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158662400-158665000	Enhancers	K562	blood
2	chr1:158665000-158667200	Weak transcription	K562	blood
3	chr1:158669800-158670000	ZNF genes & repeats	Pancreas	Pancrea
4	chr1:158676800-158677200	Enhancers	K562	blood
5	chr1:158686600-158687600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:158687000-158687600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:158687000-158687600	Enhancers	HMEC	breast
8	chr1:158687200-158687600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:158692600-158735200	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr1:158698600-158701800	Enhancers	K562	blood
11	chr1:158699200-158700400	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr1:158699600-158699800	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr1:158700200-158700600	Flanking Active TSS	Liver	Liver
14	chr1:158700400-158700600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr1:158700600-158701000	Enhancers	Liver	Liver
16	chr1:158701800-158702000	Flanking Active TSS	K562	blood
17	chr1:158701800-158702200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:158702000-158702400	Enhancers	K562	blood
19	chr1:158702400-158702800	Flanking Active TSS	K562	blood
20	chr1:158702800-158706200	Enhancers	K562	blood
21	chr1:158705600-158705800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr1:158705600-158706000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr1:158706200-158708000	Weak transcription	K562	blood
24	chr1:158708000-158708800	Enhancers	K562	blood
25	chr1:158708800-158709600	Weak transcription	K562	blood
26	chr1:158709600-158709800	Active TSS	K562	blood
27	chr1:158709800-158710000	Flanking Active TSS	K562	blood
28	chr1:158710000-158710200	Enhancers	K562	blood

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