Variant report

Variant	nsv872482
Chromosome Location	chr1:158635852-158698532
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:672)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:158654761-158655083	K562	blood:	n/a	n/a
2	ARID3A	chr1:158658785-158659538	K562	blood:	n/a	n/a
3	ARID3A	chr1:158652878-158653020	K562	blood:	n/a	n/a
4	ARID3A	chr1:158661717-158663024	K562	blood:	n/a	n/a
5	ARID3A	chr1:158656270-158657331	K562	blood:	n/a	n/a
6	ATF1	chr1:158656332-158656676	K562	blood:	n/a	n/a
7	ATF2	chr1:158685997-158686610	GM12878	blood:	n/a	n/a
8	ATF2	chr1:158685985-158686572	GM12878	blood:	n/a	n/a
9	ATF3	chr1:158656295-158656679	K562	blood:	n/a	n/a
10	BACH1	chr1:158655817-158657137	K562	blood:	n/a	n/a
11	BACH1	chr1:158656378-158656622	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr1:158686205-158686468	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:158686138-158686476	GM12878	blood:	n/a	chr1:158686264-158686273 chr1:158686265-158686274
14	BCLAF1	chr1:158686191-158686569	GM12878	blood:	n/a	chr1:158686264-158686273 chr1:158686265-158686274
15	BHLHE40	chr1:158664562-158664735	K562	blood:	n/a	n/a
16	BHLHE40	chr1:158652798-158652801	K562	blood:	n/a	n/a
17	CCNT2	chr1:158658982-158659203	K562	blood:	n/a	n/a
18	CCNT2	chr1:158661758-158662042	K562	blood:	n/a	n/a
19	CCNT2	chr1:158656386-158656746	K562	blood:	n/a	n/a
20	CEBPB	chr1:158662771-158663096	K562	blood:	n/a	n/a
21	CEBPB	chr1:158689483-158689802	K562	blood:	n/a	n/a
22	CEBPB	chr1:158659026-158659223	K562	blood:	n/a	n/a
23	CEBPB	chr1:158662761-158663125	K562	blood:	n/a	n/a
24	CEBPB	chr1:158654746-158655057	K562	blood:	n/a	n/a
25	CEBPB	chr1:158664592-158664615	K562	blood:	n/a	n/a
26	CEBPB	chr1:158656117-158657013	K562	blood:	n/a	n/a
27	CEBPB	chr1:158680689-158680944	IMR90	lung:	n/a	chr1:158680816-158680827
28	CEBPB	chr1:158680686-158680988	A549	lung:	n/a	chr1:158680816-158680827
29	CEBPB	chr1:158680693-158680923	K562	blood:	n/a	chr1:158680816-158680827
30	CEBPB	chr1:158654365-158654493	A549	lung:	n/a	n/a
31	CEBPB	chr1:158680660-158680979	HepG2	liver:	n/a	chr1:158680816-158680827
32	CEBPB	chr1:158661727-158662494	K562	blood:	n/a	n/a
33	CEBPB	chr1:158656281-158656794	K562	blood:	n/a	n/a
34	CEBPD	chr1:158661650-158662098	K562	blood:	n/a	n/a
35	CEBPD	chr1:158656260-158656754	K562	blood:	n/a	n/a
36	CEBPD	chr1:158658939-158659356	K562	blood:	n/a	n/a
37	CEBPD	chr1:158656224-158656767	K562	blood:	n/a	n/a
38	CEBPD	chr1:158658949-158659382	K562	blood:	n/a	n/a
39	CEBPD	chr1:158661791-158662138	K562	blood:	n/a	n/a
40	CHD2	chr1:158659020-158659253	K562	blood:	n/a	n/a
41	CHD2	chr1:158651271-158651421	K562	blood:	n/a	n/a
42	CTCF	chr1:158643839-158643874	Lung_OC	lung:	n/a	n/a
43	CTCF	chr1:158684800-158684950	NHEK	skin:	n/a	n/a
44	CTCF	chr1:158651410-158651451	K562	blood:	n/a	n/a
45	CTCF	chr1:158642480-158642630	GM06990	blood:	n/a	n/a
46	CTCF	chr1:158684720-158684870	GM12875	blood:	n/a	n/a
47	CTCF	chr1:158650460-158650610	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:158669880-158670030	GM12865	blood:	n/a	n/a
49	CTCF	chr1:158684680-158684830	GM12873	blood:	n/a	n/a
50	CTCF	chr1:158669730-158669755	ProgFib	skin:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158687431-158687481	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:158687431-158687481	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:158687431-158687481	SK-N-MC	brain:	n/a
4	chr1:158689263-158689313	GM19239	blood:	n/a
5	chr1:158688926-158688976	HUVEC	blood vessel:	n/a
6	chr1:158656718-158656768	H1-hESC	embryonic stem cell:	embryo
7	chr1:158670124-158670174	BJ	skin:	n/a
8	chr1:158688926-158688976	HRE	kidney:	n/a
9	chr1:158689263-158689313	RPTEC	kidney:	n/a
10	chr1:158656718-158656768	NHBE	bronchial:	n/a
11	chr1:158689263-158689313	HepG2	liver:	n/a
12	chr1:158670397-158670447	HIPEpiC	eye:	n/a
13	chr1:158687431-158687481	AG09319	gingival:	n/a
14	chr1:158687431-158687481	NHDF-neo	bronchial:	n/a
15	chr1:158689263-158689313	MCF-7	breast:	n/a
16	chr1:158671873-158671923	RPTEC	kidney:	n/a
17	chr1:158687431-158687481	RPTEC	kidney:	n/a
18	chr1:158687431-158687481	HMEC	breast:	n/a
19	chr1:158670124-158670174	H1-hESC	embryonic stem cell:	embryo
20	chr1:158688926-158688976	K562	blood:	n/a
21	chr1:158688926-158688976	T-47D	breast:	n/a
22	chr1:158670124-158670174	SK-N-MC	brain:	n/a
23	chr1:158670397-158670447	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:158688926-158688976	HNPCEpiC	eye:	n/a
25	chr1:158689263-158689313	NHDF-neo	bronchial:	n/a
26	chr1:158670617-158670667	SK-N-SH	brain:	n/a
27	chr1:158671873-158671923	HEK293	kidney:	embryo
28	chr1:158670397-158670447	AG10803	skin:	n/a
29	chr1:158656718-158656768	HRCEpiC	kidney:	n/a
30	chr1:158656718-158656768	LNCaP	prostate:	n/a
31	chr1:158671873-158671923	NHBE	bronchial:	n/a
32	chr1:158670617-158670667	NHDF-neo	bronchial:	n/a
33	chr1:158670397-158670447	PrEC	prostate:	n/a
34	chr1:158671873-158671923	Hepatocyte	liver:	n/a
35	chr1:158656718-158656768	HEK293	kidney:	embryo
36	chr1:158689263-158689313	HEEpiC	esophagus:	n/a
37	chr1:158670617-158670667	HIPEpiC	eye:	n/a
38	chr1:158656718-158656768	SK-N-MC	brain:	n/a
39	chr1:158688775-158688825	SK-N-SH_RA	brain:	n/a
40	chr1:158688775-158688825	SAEC	small airway:	n/a
41	chr1:158687431-158687481	HCM	heart:	n/a
42	chr1:158656718-158656768	ECC-1	luminal epithelium:	n/a
43	chr1:158670397-158670447	Hepatocyte	liver:	n/a
44	chr1:158688926-158688976	MCF10A-Er-Src	breast:	n/a
45	chr1:158670617-158670667	HCM	heart:	n/a
46	chr1:158688804-158688854	BE2_C	brain:	n/a
47	chr1:158689141-158689191	HCPEpiC	choroid plexus:	n/a
48	chr1:158688926-158688976	NHDF-neo	bronchial:	n/a
49	chr1:158671873-158671923	SAEC	small airway:	n/a
50	chr1:158688775-158688825	SK-N-MC	brain:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:158691383..158694379-chr1:158696049..158697811,2	K562	blood:
2	chr1:158659297..158661841-chr1:158675200..158677714,2	K562	blood:
3	chr1:158684463..158686914-chr1:158687743..158690259,2	K562	blood:
4	chr1:158649920..158652819-chr1:158694905..158696838,2	K562	blood:
5	chr1:158651585..158653705-chr1:158746762..158749250,2	K562	blood:
6	chr1:158661667..158663696-chr1:158666950..158669041,2	K562	blood:
7	chr1:158651218..158653402-chr1:158664730..158667068,2	K562	blood:
8	chr1:158659639..158662606-chr1:158667652..158670080,3	K562	blood:
9	chr1:158691573..158694598-chr1:158696049..158698060,3	K562	blood:
10	chr1:158640177..158642154-chr1:158966970..158969167,2	K562	blood:
11	chr1:158696982..158701883-chr1:158702210..158705771,7	K562	blood:
12	chr1:158653068..158654068-chr17:41445126..41445769,2	HCT-116	colon:
13	chr1:158661667..158663696-chr1:158666950..158669041,2	K562	blood:
14	chr1:158647173..158649566-chr1:158944147..158946933,2	K562	blood:
15	chr1:158691573..158694598-chr1:158696049..158698060,3	K562	blood:
16	chr1:158674913..158677154-chr1:158686436..158687990,2	K562	blood:
17	chr1:158639659..158640479-chr1:158747413..158748380,2	K562	blood:
18	chr1:158649920..158652819-chr1:158694905..158696838,2	K562	blood:
19	chr1:158631479..158633632-chr1:158637060..158639879,2	K562	blood:
20	chr1:158659639..158662606-chr1:158667652..158670080,3	K562	blood:
21	chr1:158651114..158653909-chr1:158727740..158729801,2	K562	blood:
22	chr1:158659297..158661841-chr1:158675200..158677714,2	K562	blood:
23	chr1:158653068..158653568-chr17:41445238..41445752,2	Hela-S3	cervix:
24	chr1:158676105..158677828-chr1:158684515..158686089,2	K562	blood:
25	chr1:158691383..158694379-chr1:158696049..158697811,2	K562	blood:
26	chr1:158656464..158659384-chr1:159045094..159048407,3	K562	blood:
27	chr1:158676105..158677828-chr1:158684515..158686089,2	K562	blood:
28	chr1:158697116..158699497-chr1:158702619..158704927,2	K562	blood:
29	chr1:158669887..158672800-chr1:158674715..158677591,2	K562	blood:

No data

Variant related genes	Relation type
OR6K4P	TF binding region
OR6K3	TF binding region
OR6K1P	TF binding region
OR6K2	TF binding region
SPTA1	TF binding region
OR6K4P	CpG island
OR6K3	CpG island
OR6K1P	CpG island
OR6K2	CpG island
SPTA1	CpG island
ENSG00000203757	chromatin interactions
ENSG00000163568	chromatin interactions
ENSG00000196171	chromatin interactions
ENSG00000231237	chromatin interactions
ENSG00000188340	chromatin interactions

Extended variants
information (count: 2122 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:2122 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs857680	chr1:158635852-158635853	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs71579625	chr1:158635853-158635854	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180882130	chr1:158635860-158635861	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56362544	chr1:158635875-158635876	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs552891084	chr1:158635879-158635880	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572738732	chr1:158635900-158635901	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545320279	chr1:158635919-158635920	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375572270	chr1:158635937-158635938	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571072886	chr1:158635957-158635958	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564814954	chr1:158635986-158635987	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs56330526	chr1:158636010-158636011	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs184841353	chr1:158636013-158636014	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568498610	chr1:158636041-158636042	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535544776	chr1:158636045-158636046	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111393509	chr1:158636046-158636047	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571886325	chr1:158636050-158636051	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376085101	chr1:158636058-158636059	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189778672	chr1:158636074-158636075	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369474872	chr1:158636075-158636076	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373646521	chr1:158636079-158636080	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145972324	chr1:158636110-158636111	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199544164	chr1:158636111-158636112	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370468407	chr1:158636114-158636115	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376278222	chr1:158636121-158636122	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377362395	chr1:158636122-158636123	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200438116	chr1:158636144-158636145	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543365746	chr1:158636150-158636151	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375230030	chr1:158636152-158636153	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368012895	chr1:158636157-158636158	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561521001	chr1:158636165-158636166	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199815523	chr1:158636166-158636167	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371855997	chr1:158636181-158636182	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12090314	chr1:158636224-158636225	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs201048261	chr1:158636225-158636226	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372728613	chr1:158636227-158636228	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375568203	chr1:158636235-158636236	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200589641	chr1:158636253-158636254	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181529699	chr1:158636296-158636297	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368915704	chr1:158636314-158636315	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371350614	chr1:158636320-158636321	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562972789	chr1:158636420-158636421	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546439762	chr1:158636425-158636426	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561057778	chr1:158636498-158636499	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143401540	chr1:158636533-158636534	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531917941	chr1:158636575-158636576	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530162842	chr1:158636579-158636580	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550490957	chr1:158636668-158636669	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576230177	chr1:158636679-158636680	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543606583	chr1:158636716-158636717	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs58195064	chr1:158636725-158636726	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:110)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158634400-158652800	Strong transcription	K562	blood
2	chr1:158641000-158642000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:158644400-158645400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
4	chr1:158644400-158645400	Enhancers	Primary hematopoietic stem cells	blood
5	chr1:158644400-158645400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
6	chr1:158644400-158646800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:158644600-158646600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:158644800-158646200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:158645200-158646600	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr1:158645800-158646200	Enhancers	Fetal Thymus	thymus
11	chr1:158651000-158652200	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr1:158651200-158652200	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr1:158652200-158656200	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr1:158652800-158655200	Transcr. at gene 5' and 3'	K562	blood
15	chr1:158655200-158655400	Bivalent/Poised TSS	Primary T helper 17 cells PMA-I stimulated	--
16	chr1:158655200-158657000	Active TSS	K562	blood
17	chr1:158655800-158656200	Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr1:158655800-158657000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:158656000-158656600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:158656000-158656800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:158656200-158656400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
22	chr1:158656200-158656400	Enhancers	A549	lung
23	chr1:158656200-158656600	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr1:158656200-158656800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:158656200-158657000	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr1:158656400-158657200	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr1:158657000-158657400	Flanking Active TSS	K562	blood
28	chr1:158657400-158657800	Enhancers	K562	blood
29	chr1:158657800-158658800	Weak transcription	K562	blood
30	chr1:158658800-158659000	Active TSS	K562	blood
31	chr1:158659000-158660000	Flanking Active TSS	K562	blood
32	chr1:158660000-158660800	Enhancers	K562	blood
33	chr1:158660800-158661600	Weak transcription	K562	blood
34	chr1:158661600-158661800	Active TSS	K562	blood
35	chr1:158661800-158662000	Flanking Active TSS	K562	blood
36	chr1:158662000-158662200	Active TSS	K562	blood
37	chr1:158662200-158662400	Flanking Active TSS	K562	blood
38	chr1:158662400-158665000	Enhancers	K562	blood
39	chr1:158665000-158667200	Weak transcription	K562	blood
40	chr1:158669800-158670000	ZNF genes & repeats	Pancreas	Pancrea
41	chr1:158676800-158677200	Enhancers	K562	blood
42	chr1:158686600-158687600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:158687000-158687600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr1:158687000-158687600	Enhancers	HMEC	breast
45	chr1:158687200-158687600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:158692600-158735200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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