Variant report

Variant	esv3523372
Chromosome Location	chr1:144453745-144501843
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:411)
CpG islands
(count:244)
Chromatin interactive
region (count:0)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:144490172-144490373	GM12878	blood:	n/a	n/a
2	BATF	chr1:144501613-144502087	GM12878	blood:	n/a	n/a
3	BATF	chr1:144501231-144502049	GM12878	blood:	n/a	chr1:144501567-144501576
4	BATF	chr1:144490944-144491993	GM12878	blood:	n/a	n/a
5	BATF	chr1:144491160-144491907	GM12878	blood:	n/a	n/a
6	BATF	chr1:144494382-144494639	GM12878	blood:	n/a	n/a
7	BATF	chr1:144492553-144492818	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:144501244-144501475	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:144494424-144494661	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:144501616-144502097	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:144501589-144502064	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:144494397-144494666	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:144491151-144491757	GM12878	blood:	n/a	chr1:144491623-144491632
14	BCL11A	chr1:144501112-144501338	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:144492541-144492795	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:144490839-144491806	GM12878	blood:	n/a	chr1:144491623-144491632
17	CBX3	chr1:144491147-144492044	K562	blood:	n/a	n/a
18	CBX3	chr1:144491177-144491694	K562	blood:	n/a	n/a
19	CBX3	chr1:144464027-144464319	K562	blood:	n/a	n/a
20	CEBPB	chr1:144494152-144494438	K562	blood:	n/a	n/a
21	CEBPB	chr1:144494062-144494535	K562	blood:	n/a	n/a
22	CEBPB	chr1:144491338-144491570	GM12878	blood:	n/a	n/a
23	CEBPB	chr1:144491160-144491917	GM12878	blood:	n/a	n/a
24	CEBPB	chr1:144491079-144491764	K562	blood:	n/a	n/a
25	CEBPB	chr1:144496597-144496884	K562	blood:	n/a	n/a
26	CEBPB	chr1:144496528-144496881	K562	blood:	n/a	n/a
27	CEBPD	chr1:144482920-144483117	K562	blood:	n/a	n/a
28	CEBPD	chr1:144494037-144494572	K562	blood:	n/a	n/a
29	CEBPD	chr1:144490979-144491939	K562	blood:	n/a	n/a
30	CTCF	chr1:144453865-144454030	A549	lung:	n/a	n/a
31	CTCF	chr1:144460798-144460855	GM20000	blood:	n/a	n/a
32	CTCF	chr1:144478486-144478548	LNCaP	prostate:	n/a	n/a
33	CTCF	chr1:144456416-144456465	GM10248	blood:	n/a	n/a
34	CTCF	chr1:144453830-144454140	K562	blood:	n/a	n/a
35	CTCF	chr1:144478358-144478473	GM20000	blood:	n/a	n/a
36	CTCF	chr1:144453880-144454030	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr1:144467316-144467375	LNCaP	prostate:	n/a	n/a
38	CTCF	chr1:144453815-144454026	K562	blood:	n/a	n/a
39	CTCF	chr1:144476472-144476541	Medullo	brain:	n/a	n/a
40	CTCF	chr1:144482816-144482916	LNCaP	prostate:	n/a	n/a
41	CTCF	chr1:144491704-144491851	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr1:144456865-144456936	GM10248	blood:	n/a	n/a
43	CTCF	chr1:144453813-144454138	A549	lung:	n/a	n/a
44	CTCF	chr1:144481717-144481784	LNCaP	prostate:	n/a	n/a
45	CTCF	chr1:144475434-144475498	GM10248	blood:	n/a	n/a
46	CTCF	chr1:144483423-144483481	Medullo	brain:	n/a	n/a
47	CTCF	chr1:144454545-144454614	GM10248	blood:	n/a	n/a
48	CTCF	chr1:144461198-144461264	GM20000	blood:	n/a	n/a
49	CTCF	chr1:144453814-144454067	K562	blood:	n/a	n/a
50	CTCF	chr1:144481249-144481566	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144481939-144481989	Caco-2	colon:	n/a
2	chr1:144485590-144485640	AG09319	gingival:	n/a
3	chr1:144481939-144481989	HEK293	kidney:	embryo
4	chr1:144489264-144489314	HIPEpiC	eye:	n/a
5	chr1:144481939-144481989	PFSK-1	brain:	n/a
6	chr1:144489264-144489314	AG09319	gingival:	n/a
7	chr1:144485590-144485640	MCF10A-Er-Src	breast:	n/a
8	chr1:144489264-144489314	MCF10A-Er-Src	breast:	n/a
9	chr1:144479586-144479636	Hela-S3	cervix:	n/a
10	chr1:144485590-144485640	AG10803	skin:	n/a
11	chr1:144479586-144479636	HRPEpiC	eye:	n/a
12	chr1:144489264-144489314	Caco-2	colon:	n/a
13	chr1:144485590-144485640	AoSMC	blood vessel:	n/a
14	chr1:144485590-144485640	GM12878	blood:	n/a
15	chr1:144489264-144489314	Hela-S3	cervix:	n/a
16	chr1:144481939-144481989	HEEpiC	esophagus:	n/a
17	chr1:144485590-144485640	HCM	heart:	n/a
18	chr1:144481939-144481989	AoSMC	blood vessel:	n/a
19	chr1:144479586-144479636	NHDF-neo	bronchial:	n/a
20	chr1:144481939-144481989	HAEpiC	amniotic membrane:	n/a
21	chr1:144479586-144479636	HCM	heart:	n/a
22	chr1:144479586-144479636	MCF-7	breast:	n/a
23	chr1:144481939-144481989	NHDF-neo	bronchial:	n/a
24	chr1:144481939-144481989	SK-N-SH_RA	brain:	n/a
25	chr1:144481939-144481989	SKMC	muscle:	n/a
26	chr1:144489264-144489314	HCM	heart:	n/a
27	chr1:144485590-144485640	SK-N-SH_RA	brain:	n/a
28	chr1:144489264-144489314	ECC-1	luminal epithelium:	n/a
29	chr1:144489264-144489314	HCPEpiC	choroid plexus:	n/a
30	chr1:144481939-144481989	GM12878	blood:	n/a
31	chr1:144485590-144485640	GM12891	blood:	n/a
32	chr1:144479586-144479636	ECC-1	luminal epithelium:	n/a
33	chr1:144485590-144485640	U87	brain:	n/a
34	chr1:144481939-144481989	HCPEpiC	choroid plexus:	n/a
35	chr1:144479586-144479636	RPTEC	kidney:	n/a
36	chr1:144479586-144479636	BE2_C	brain:	n/a
37	chr1:144489264-144489314	RPTEC	kidney:	n/a
38	chr1:144481939-144481989	HRCEpiC	kidney:	n/a
39	chr1:144485590-144485640	K562	blood:	n/a
40	chr1:144489264-144489314	HRPEpiC	eye:	n/a
41	chr1:144485590-144485640	HepG2	liver:	n/a
42	chr1:144489264-144489314	AG10803	skin:	n/a
43	chr1:144485590-144485640	Caco-2	colon:	n/a
44	chr1:144489264-144489314	NHBE	bronchial:	n/a
45	chr1:144481939-144481989	ProgFib	skin:	n/a
46	chr1:144479586-144479636	HRE	kidney:	n/a
47	chr1:144485590-144485640	SK-N-SH	brain:	n/a
48	chr1:144481939-144481989	HIPEpiC	eye:	n/a
49	chr1:144485590-144485640	PFSK-1	brain:	n/a
50	chr1:144489264-144489314	HCF	heart:	n/a

No data

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPIAL4B-2	chr1:144480744-144481765	ENSG00000236943.1
2	lnc-PPIAL4B-5	chr1:144475088-144475533	predAs_chen_AA985444_1
3	lnc-PPIAL4B-2	chr1:144461309-144461412	ENSG00000236943.1
4	lnc-PPIAL4B-2	chr1:144481627-144481765	ENSG00000236943.1
5	lnc-PPIAL4B-2	chr1:144480746-144480984	NONHSAT005803
6	lnc-PPIAL4B-2	chr1:144481419-144481765	NONHSAT005803
7	lnc-PPIAL4B-2	chr1:144460973-144461111	ENSG00000236943.1
8	lnc-PPIAL4B-2	chr1:144460626-144460872	ENSG00000236943.1
9	lnc-PPIAL4B-2	chr1:144480741-144480984	ENSG00000236943.1
10	lnc-PPIAL4B-2	chr1:144481419-144481765	ENSG00000236943.1

No data

Variant related genes	Relation type
RNVU1-5	TF binding region
ENSG00000236943	TF binding region
RNVU1-5	CpG island
ENSG00000236943	CpG island

Extended variants
information (count: 46 )
Associated
traits (count: 166 )

Variant overlapped rSNPs/rCNVs (count:46 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587749648	chr1:144461391-144461392	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs202175219	chr1:144462256-144462257	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs199614711	chr1:144462560-144462561	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs200791081	chr1:144462599-144462600	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs201731836	chr1:144462623-144462624	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs199525959	chr1:144462800-144462801	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs200080124	chr1:144462803-144462804	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs587640545	chr1:144462870-144462871	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs200520974	chr1:144462879-144462880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200065566	chr1:144462907-144462908	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs587718557	chr1:144462953-144462954	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs201510313	chr1:144462975-144462976	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs201069886	chr1:144463314-144463315	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs587595647	chr1:144475210-144475211	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs370609531	chr1:144475230-144475231	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs587670252	chr1:144475239-144475240	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs371232376	chr1:144475420-144475421	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs587699441	chr1:144475437-144475438	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs376158718	chr1:144475474-144475475	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs200465849	chr1:144480794-144480795	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs376417394	chr1:144481110-144481111	Active TSS Enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
22	rs587775534	chr1:144481182-144481183	Active TSS Enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
23	rs116180770	chr1:144481200-144481201	Active TSS Enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	mRNA abundance
24	rs587662116	chr1:144481219-144481220	Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs587719553	chr1:144481233-144481234	Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs139706301	chr1:144481235-144481236	Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs200307645	chr1:144483423-144483424	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs187648996	chr1:144485616-144485617	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs372443997	chr1:144491691-144491692	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs587639730	chr1:144491937-144491938	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs587723604	chr1:144491964-144491965	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs587773470	chr1:144492766-144492767	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs587626825	chr1:144492824-144492825	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs587690275	chr1:144492840-144492841	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs376349822	chr1:144493626-144493627	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs3009807	chr1:144494054-144494055	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs2923190	chr1:144494824-144494825	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs56334001	chr1:144494862-144494863	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs2994171	chr1:144495026-144495027	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs200917218	chr1:144495498-144495499	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs7414954	chr1:144495549-144495550	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs587746460	chr1:144495555-144495556	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs7417211	chr1:144495604-144495605	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs7416255	chr1:144495614-144495615	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs7415421	chr1:144495747-144495748	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs376810194	chr1:144495818-144495819	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:166)

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
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	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
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	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
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
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	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
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	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
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	20967226	CNVD
Autism	20841430	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144481000-144481200	ZNF genes & repeats	Lung	lung
2	chr1:144481000-144481400	Active TSS	H1 Cell Line	embryonic stem cell
3	chr1:144481000-144481400	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr1:144481000-144481400	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr1:144481000-144481400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:144481000-144481400	Active TSS	Primary T cells fromperipheralblood	blood
7	chr1:144481000-144481400	Active TSS	Primary T helper cells fromperipheralblood	blood
8	chr1:144481000-144481400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr1:144481000-144481400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:144481000-144481400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:144481000-144481400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:144481000-144481400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:144481000-144481400	Active TSS	Brain Germinal Matrix	brain
14	chr1:144481000-144481400	Active TSS	Fetal Brain Female	brain
15	chr1:144481000-144481400	Active TSS	Fetal Intestine Small	intestine
16	chr1:144481000-144481400	Active TSS	Thymus	Thymus
17	chr1:144481000-144481400	Active TSS	Monocytes-CD14+_RO01746	blood
18	chr1:144491800-144492200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:144491800-144492200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:144491800-144492200	Active TSS	Fetal Thymus	thymus
21	chr1:144491800-144492200	Active TSS	Monocytes-CD14+_RO01746	blood
22	chr1:144491800-144492200	Active TSS	Osteobl	bone

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