Variant report

Variant	esv2764266
Chromosome Location	chr1:158700732-158725880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:306)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:77 , 50 per page) page: 1 2

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	chr1:158709982-158710193	K562	blood:	n/a	n/a
3	ARID3A	chr1:158702324-158702669	K562	blood:	n/a	n/a
4	BACH1	chr1:158701798-158702048	K562	blood:	n/a	n/a
5	BHLHE40	chr1:158701588-158702091	K562	blood:	n/a	n/a
6	CEBPB	chr1:158722945-158723184	H1-hESC	embryonic stem cell:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
7	CEBPB	chr1:158722946-158723214	HepG2	liver:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
8	CEBPB	chr1:158722931-158723169	IMR90	lung:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
9	CEBPB	chr1:158722871-158723208	K562	blood:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
10	CEBPB	chr1:158719042-158719256	HepG2	liver:	n/a	chr1:158719183-158719196 chr1:158719183-158719194
11	CEBPB	chr1:158719103-158719306	A549	lung:	n/a	chr1:158719183-158719196 chr1:158719183-158719194
12	CEBPB	chr1:158711092-158711357	K562	blood:	n/a	n/a
13	CEBPB	chr1:158705115-158705187	K562	blood:	n/a	n/a
14	CEBPB	chr1:158722864-158723064	A549	lung:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
15	CEBPB	chr1:158722942-158723176	Hela-S3	cervix:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
16	CEBPD	chr1:158702210-158702773	K562	blood:	n/a	n/a
17	CEBPD	chr1:158702247-158702768	K562	blood:	n/a	n/a
18	CHD2	chr1:158707497-158707550	K562	blood:	n/a	n/a
19	CTCF	chr1:158703490-158703560	GM20000	blood:	n/a	n/a
20	CTCF	chr1:158722200-158722406	K562	blood:	n/a	n/a
21	CTCF	chr1:158722251-158722361	K562	blood:	n/a	n/a
22	E2F4	chr1:158711498-158711698	MCF10A-Er-Src	breast:	n/a	n/a
23	EBF1	chr1:158703222-158703483	GM12878	blood:	n/a	chr1:158703323-158703334
24	EP300	chr1:158708315-158708350	K562	blood:	n/a	n/a
25	EP300	chr1:158701733-158702739	K562	blood:	n/a	n/a
26	FOS	chr1:158711099-158711423	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr1:158711179-158711378	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:158711096-158711426	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr1:158711089-158711418	MCF10A-Er-Src	breast:	n/a	n/a
30	GATA1	chr1:158701669-158703049	PBDE	blood:	n/a	n/a
31	GATA1	chr1:158701610-158702854	K562	blood:	n/a	n/a
32	GATA1	chr1:158713956-158714405	PBDE	blood:	n/a	n/a
33	GATA2	chr1:158702273-158702678	K562	blood:	n/a	n/a
34	GTF2B	chr1:158703657-158703957	K562	blood:	n/a	n/a
35	HCFC1	chr1:158710216-158710334	K562	blood:	n/a	n/a
36	IRF1	chr1:158702162-158702644	K562	blood:	n/a	n/a
37	IRF1	chr1:158708175-158708320	K562	blood:	n/a	n/a
38	IRF1	chr1:158700228-158700835	K562	blood:	n/a	chr1:158700449-158700470
39	JUN	chr1:158705356-158705898	K562	blood:	n/a	n/a
40	JUND	chr1:158710040-158710132	K562	blood:	n/a	n/a
41	JUND	chr1:158701502-158702695	K562	blood:	n/a	n/a
42	JUND	chr1:158705212-158705235	K562	blood:	n/a	n/a
43	MAFK	chr1:158713233-158713398	HepG2	liver:	n/a	n/a
44	MAFK	chr1:158711748-158711948	HepG2	liver:	n/a	chr1:158711865-158711885
45	MAFK	chr1:158713144-158713371	HepG2	liver:	n/a	n/a
46	MAFK	chr1:158709573-158709727	HepG2	liver:	n/a	n/a
47	MAX	chr1:158701488-158701801	K562	blood:	n/a	n/a
48	MXI1	chr1:158709411-158709426	K562	blood:	n/a	n/a
49	MYC	chr1:158701594-158701767	K562	blood:	n/a	n/a
50	NR2F2	chr1:158702383-158702674	K562	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158725300-158725350	H1-hESC	embryonic stem cell:	embryo
2	chr1:158725300-158725350	H1-hESC	embryonic stem cell:	embryo
3	chr1:158723939-158723989	LNCaP	prostate:	n/a
4	chr1:158723939-158723989	ECC-1	luminal epithelium:	n/a
5	chr1:158723939-158723989	Jurkat	blood:	n/a
6	chr1:158723939-158723989	HUVEC	blood vessel:	n/a
7	chr1:158725300-158725350	CMK	blood:	n/a
8	chr1:158724794-158724844	CMK	blood:	n/a
9	chr1:158725300-158725350	NB4	blood:	n/a
10	chr1:158724794-158724844	MCF10A-Er-Src	breast:	n/a
11	chr1:158723939-158723989	SK-N-MC	brain:	n/a
12	chr1:158723939-158723989	HEK293	kidney:	embryo
13	chr1:158723939-158723989	MCF10A-Er-Src	breast:	n/a
14	chr1:158725300-158725350	HMEC	breast:	n/a
15	chr1:158724794-158724844	HMEC	breast:	n/a
16	chr1:158724794-158724844	HUVEC	blood vessel:	n/a
17	chr1:158724362-158724412	GM19239	blood:	n/a
18	chr1:158723939-158723989	RPTEC	kidney:	n/a
19	chr1:158724362-158724412	CMK	blood:	n/a
20	chr1:158723939-158723989	HL-60	blood:	n/a
21	chr1:158724057-158724107	HCM	heart:	n/a
22	chr1:158725300-158725350	GM12878	blood:	n/a
23	chr1:158725300-158725350	RPTEC	kidney:	n/a
24	chr1:158725300-158725350	HRE	kidney:	n/a
25	chr1:158724362-158724412	HCPEpiC	choroid plexus:	n/a
26	chr1:158724794-158724844	ECC-1	luminal epithelium:	n/a
27	chr1:158725300-158725350	GM12892	blood:	n/a
28	chr1:158724057-158724107	GM12878	blood:	n/a
29	chr1:158724362-158724412	HRE	kidney:	n/a
30	chr1:158724057-158724107	AG09319	gingival:	n/a
31	chr1:158724794-158724844	PFSK-1	brain:	n/a
32	chr1:158724057-158724107	HRPEpiC	eye:	n/a
33	chr1:158724057-158724107	MCF10A-Er-Src	breast:	n/a
34	chr1:158725300-158725350	Caco-2	colon:	n/a
35	chr1:158725300-158725350	HCT-116	colon:	n/a
36	chr1:158725300-158725350	AG09319	gingival:	n/a
37	chr1:158724362-158724412	Jurkat	blood:	n/a
38	chr1:158725300-158725350	HEK293	kidney:	embryo
39	chr1:158723939-158723989	HCPEpiC	choroid plexus:	n/a
40	chr1:158724794-158724844	BJ	skin:	n/a
41	chr1:158724362-158724412	SKMC	muscle:	n/a
42	chr1:158724362-158724412	NB4	blood:	n/a
43	chr1:158723939-158723989	NHDF-neo	bronchial:	n/a
44	chr1:158724057-158724107	PrEC	prostate:	n/a
45	chr1:158725300-158725350	T-47D	breast:	n/a
46	chr1:158724362-158724412	LNCaP	prostate:	n/a
47	chr1:158724057-158724107	NT2-D1	testis:	n/a
48	chr1:158724362-158724412	BE2_C	brain:	n/a
49	chr1:158724362-158724412	RPTEC	kidney:	n/a
50	chr1:158725300-158725350	BE2_C	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:158715265..158717778-chr1:158778694..158781362,2	K562	blood:
2	chr1:158699118..158701949-chr1:158709331..158711984,2	K562	blood:
3	chr1:158696982..158701883-chr1:158702210..158705771,7	K562	blood:
4	chr1:158699118..158701949-chr1:158709331..158711984,2	K562	blood:
5	chr1:158701755..158705583-chr1:158706296..158709041,3	K562	blood:
6	chr1:158711568..158713375-chr1:158713499..158715477,2	K562	blood:
7	chr1:158702009..158703945-chr1:158717255..158718973,2	K562	blood:
8	chr1:158697116..158699497-chr1:158702619..158704927,2	K562	blood:
9	chr1:158696982..158701883-chr1:158702210..158705771,7	K562	blood:
10	chr1:158704822..158706927-chr1:158777581..158780196,2	K562	blood:
11	chr1:158701755..158705583-chr1:158706296..158709041,3	K562	blood:
12	chr1:158702009..158703945-chr1:158717255..158718973,2	K562	blood:
13	chr1:158701358..158703864-chr1:158711036..158713684,2	K562	blood:
14	chr1:158653549..158656527-chr1:158701529..158703994,2	K562	blood:

No data

Variant related genes	Relation type
OR6K5P	TF binding region
OR6K6	TF binding region
OR6K5P	CpG island
OR6K6	CpG island
ENSG00000163554	chromatin interactions
ENSG00000180409	chromatin interactions
ENSG00000226949	chromatin interactions

Extended variants
information (count: 1056 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1056 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs703147	chr1:158700732-158700733	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538397388	chr1:158700856-158700857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550110487	chr1:158700861-158700862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568710034	chr1:158700909-158700910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs703148	chr1:158700972-158700973	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs326005	chr1:158701010-158701011	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs187373441	chr1:158701011-158701012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192090399	chr1:158701018-158701019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558190383	chr1:158701019-158701020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369853513	chr1:158701024-158701025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576462237	chr1:158701026-158701027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543573511	chr1:158701038-158701039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs386635929	chr1:158701058-158701059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201784130	chr1:158701067-158701068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374274020	chr1:158701071-158701072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369760474	chr1:158701072-158701073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs74403289	chr1:158701096-158701097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs326006	chr1:158701200-158701201	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs540907590	chr1:158701229-158701230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559271641	chr1:158701240-158701241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532758549	chr1:158701298-158701299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375925039	chr1:158701320-158701321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74427709	chr1:158701321-158701322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563349334	chr1:158701417-158701418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs16840748	chr1:158701420-158701421	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs1930261	chr1:158701449-158701450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs568656502	chr1:158701466-158701467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565731614	chr1:158701472-158701473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs370851129	chr1:158701523-158701524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs140451900	chr1:158701525-158701526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs113369942	chr1:158701603-158701604	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs374156557	chr1:158701614-158701615	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs77800865	chr1:158701660-158701661	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs539796820	chr1:158701661-158701662	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs150393890	chr1:158701662-158701663	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs570097264	chr1:158701725-158701726	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs145269356	chr1:158701732-158701733	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs326007	chr1:158701762-158701763	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs549787375	chr1:158701785-158701786	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs78865107	chr1:158701817-158701818	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs1953068	chr1:158701841-158701842	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs183396253	chr1:158701861-158701862	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs149160327	chr1:158701875-158701876	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs544961156	chr1:158701900-158701901	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576247442	chr1:158701904-158701905	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs563153667	chr1:158701910-158701911	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs115366506	chr1:158701978-158701979	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs146851315	chr1:158702032-158702033	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs186598181	chr1:158702047-158702048	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112837228	chr1:158702080-158702081	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	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
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
Breast cancer	22522925	CNVD

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158692600-158735200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr1:158698600-158701800	Enhancers	K562	blood
3	chr1:158700600-158701000	Enhancers	Liver	Liver
4	chr1:158701800-158702000	Flanking Active TSS	K562	blood
5	chr1:158701800-158702200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:158702000-158702400	Enhancers	K562	blood
7	chr1:158702400-158702800	Flanking Active TSS	K562	blood
8	chr1:158702800-158706200	Enhancers	K562	blood
9	chr1:158705600-158705800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:158705600-158706000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr1:158706200-158708000	Weak transcription	K562	blood
12	chr1:158708000-158708800	Enhancers	K562	blood
13	chr1:158708800-158709600	Weak transcription	K562	blood
14	chr1:158709600-158709800	Active TSS	K562	blood
15	chr1:158709800-158710000	Flanking Active TSS	K562	blood
16	chr1:158710000-158710200	Enhancers	K562	blood
17	chr1:158721800-158722200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:158722400-158724800	Enhancers	Fetal Heart	heart

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