Variant report

Variant	nsv879013
Chromosome Location	chr4:54093717-54137228
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:111)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:111 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:54101654-54102139	GM12878	blood:	n/a	n/a
2	ATF2	chr4:54101556-54102252	GM12878	blood:	n/a	n/a
3	BATF	chr4:54101615-54102107	GM12878	blood:	n/a	n/a
4	BATF	chr4:54101676-54102017	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:54101704-54102148	GM12878	blood:	n/a	n/a
6	BCL11A	chr4:54101719-54102017	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:54101712-54102092	GM12878	blood:	n/a	n/a
8	CEBPB	chr4:54131944-54132027	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD1	chr4:54101231-54101239	GM12878	blood:	n/a	n/a
10	CHD2	chr4:54101803-54102105	GM12878	blood:	n/a	n/a
11	CHD2	chr4:54101363-54101530	GM12878	blood:	n/a	n/a
12	CTCF	chr4:54129813-54129978	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr4:54125992-54126037	GM13976	blood:	n/a	n/a
14	CTCF	chr4:54099360-54099510	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr4:54111518-54111566	LNCaP	prostate:	n/a	n/a
16	CTCF	chr4:54129868-54129875	GM19240	blood:	n/a	n/a
17	CTCF	chr4:54099380-54099530	HPF	lung:	n/a	n/a
18	CTCF	chr4:54099340-54099490	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr4:54129880-54129903	GM19240	blood:	n/a	n/a
20	CTCF	chr4:54129784-54129895	GM10248	blood:	n/a	n/a
21	CTCF	chr4:54099340-54099490	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr4:54129860-54130010	HepG2	liver:	n/a	n/a
23	CTCF	chr4:54129125-54129217	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr4:54129930-54129983	GM20000	blood:	n/a	n/a
25	CTCF	chr4:54110783-54110844	GM13976	blood:	n/a	n/a
26	CTCF	chr4:54099520-54099670	AG09319	gingival:	n/a	n/a
27	CTCF	chr4:54129906-54129914	GM19240	blood:	n/a	n/a
28	CTCF	chr4:54129820-54129970	GM12864	blood:	n/a	n/a
29	CTCF	chr4:54129840-54129990	BE2_C	brain:	n/a	n/a
30	CTCF	chr4:54129872-54129886	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:54129897-54129935	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:54134857-54134909	Fibrobl	skin:	n/a	n/a
33	CUX1	chr4:54101494-54102067	GM12878	blood:	n/a	n/a
34	E2F4	chr4:54136701-54136815	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr4:54100676-54100793	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr4:54101759-54102057	GM12878	blood:	n/a	n/a
37	EP300	chr4:54101434-54102131	GM12878	blood:	n/a	n/a
38	FOS	chr4:54100854-54101175	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:54093733-54093867	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:54100845-54101166	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr4:54100813-54101196	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr4:54100874-54101130	MCF10A-Er-Src	breast:	n/a	n/a
43	FOXA1	chr4:54114283-54114633	HepG2	liver:	n/a	n/a
44	FOXA2	chr4:54114424-54114607	HepG2	liver:	n/a	n/a
45	FOXA2	chr4:54114289-54114836	A549	lung:	n/a	n/a
46	FOXA2	chr4:54122688-54123089	A549	lung:	n/a	n/a
47	GATA1	chr4:54094047-54094670	PBDE	blood:	n/a	chr4:54094469-54094485 chr4:54094469-54094485
48	GATA2	chr4:54124089-54124335	HUVEC	blood vessel:	n/a	chr4:54124126-54124134 chr4:54124194-54124203 chr4:54124189-54124203
49	IRF1	chr4:54106727-54106735	K562	blood:	n/a	n/a
50	IRF1	chr4:54097551-54097733	K562	blood:	n/a	chr4:54097678-54097688 chr4:54097674-54097688

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:54104209-54104259	HL-60	blood:	n/a
2	chr4:54104209-54104259	NHDF-neo	bronchial:	n/a
3	chr4:54104209-54104259	SK-N-MC	brain:	n/a
4	chr4:54104209-54104259	Hela-S3	cervix:	n/a
5	chr4:54104209-54104259	AG04450	lung:	fetal
6	chr4:54104209-54104259	AG09309	skin:	n/a
7	chr4:54104209-54104259	Hepatocyte	liver:	n/a
8	chr4:54104209-54104259	Jurkat	blood:	n/a
9	chr4:54104209-54104259	GM12878	blood:	n/a
10	chr4:54104209-54104259	HEK293	kidney:	embryo
11	chr4:54104209-54104259	Caco-2	colon:	n/a
12	chr4:54104209-54104259	A549	lung:	n/a
13	chr4:54104209-54104259	HRCEpiC	kidney:	n/a
14	chr4:54104209-54104259	AG10803	skin:	n/a
15	chr4:54104209-54104259	HCPEpiC	choroid plexus:	n/a
16	chr4:54104209-54104259	HEEpiC	esophagus:	n/a
17	chr4:54104209-54104259	ProgFib	skin:	n/a
18	chr4:54104209-54104259	HRE	kidney:	n/a
19	chr4:54104209-54104259	HIPEpiC	eye:	n/a
20	chr4:54104209-54104259	SAEC	small airway:	n/a
21	chr4:54104209-54104259	NH-A	brain:	n/a
22	chr4:54104209-54104259	CMK	blood:	n/a
23	chr4:54104209-54104259	K562	blood:	n/a
24	chr4:54104209-54104259	PANC-1	pancreas:	n/a
25	chr4:54104209-54104259	ovcar-3	ovarian:	n/a
26	chr4:54104209-54104259	GM06990	blood:	n/a
27	chr4:54104209-54104259	U87	brain:	n/a
28	chr4:54104209-54104259	HMEC	breast:	n/a
29	chr4:54104209-54104259	AoSMC	blood vessel:	n/a
30	chr4:54104209-54104259	T-47D	breast:	n/a
31	chr4:54104209-54104259	MCF-7	breast:	n/a
32	chr4:54104209-54104259	PrEC	prostate:	n/a
33	chr4:54104209-54104259	GM12891	blood:	n/a
34	chr4:54104209-54104259	BE2_C	brain:	n/a
35	chr4:54104209-54104259	HepG2	liver:	n/a
36	chr4:54104209-54104259	NB4	blood:	n/a
37	chr4:54104209-54104259	BJ	skin:	n/a
38	chr4:54104209-54104259	HNPCEpiC	eye:	n/a
39	chr4:54104209-54104259	HAEpiC	amniotic membrane:	n/a
40	chr4:54104209-54104259	AG09319	gingival:	n/a
41	chr4:54104209-54104259	HRPEpiC	eye:	n/a
42	chr4:54104209-54104259	LNCaP	prostate:	n/a
43	chr4:54104209-54104259	HCT-116	colon:	n/a
44	chr4:54104209-54104259	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:54104209-54104259	HCF	heart:	n/a
46	chr4:54104209-54104259	HUVEC	blood vessel:	n/a
47	chr4:54104209-54104259	PFSK-1	brain:	n/a
48	chr4:54104209-54104259	IMR90	lung:	fetal
49	chr4:54104209-54104259	SK-N-SH	brain:	n/a
50	chr4:54104209-54104259	GM19239	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:54124166..54126954-chr4:54482299..54484673,2	K562	blood:
2	chr4:54107331..54109180-chr4:54137571..54139298,2	K562	blood:
3	chr15:88111468..88112097-chr4:54099120..54099988,2	MCF-7	breast:
4	chr4:54130628..54132899-chr4:54134873..54136531,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-310P	TF binding region
RNU6-310P	CpG island
ENSG00000072201	chromatin interactions
ENSG00000207385	chromatin interactions

Extended variants
information (count: 1923 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1923 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2412401	chr4:54093717-54093718	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141611932	chr4:54093768-54093769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573631872	chr4:54093784-54093785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528077612	chr4:54093794-54093795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559349426	chr4:54093824-54093825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150754694	chr4:54093901-54093902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546259400	chr4:54093903-54093904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571023055	chr4:54093924-54093925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544861432	chr4:54093945-54093946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551657574	chr4:54093955-54093956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565419363	chr4:54093962-54093963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12509702	chr4:54093969-54093970	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs550616485	chr4:54094068-54094069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115465264	chr4:54094077-54094078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530004117	chr4:54094120-54094121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138887968	chr4:54094140-54094141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76021594	chr4:54094154-54094155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12505661	chr4:54094203-54094204	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs367933552	chr4:54094265-54094266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558872834	chr4:54094267-54094268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571413897	chr4:54094283-54094284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565977198	chr4:54094288-54094289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191753856	chr4:54094309-54094310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569082928	chr4:54094321-54094322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149416761	chr4:54094328-54094329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376530157	chr4:54094361-54094362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114973439	chr4:54094382-54094383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77685174	chr4:54094404-54094405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553267941	chr4:54094409-54094410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573045102	chr4:54094432-54094433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536149301	chr4:54094454-54094455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545236039	chr4:54094476-54094477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554648210	chr4:54094495-54094496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2412402	chr4:54094528-54094529	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs575058299	chr4:54094537-54094538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376524366	chr4:54094547-54094548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544317552	chr4:54094583-54094584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116053220	chr4:54094620-54094621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530063116	chr4:54094639-54094640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546660954	chr4:54094672-54094673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114852121	chr4:54094673-54094674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184718469	chr4:54094676-54094677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553470987	chr4:54094678-54094679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144788166	chr4:54094681-54094682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569481993	chr4:54094684-54094685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538405951	chr4:54094716-54094717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188993209	chr4:54094737-54094738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148576135	chr4:54094738-54094739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567354965	chr4:54094781-54094782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3986374	chr4:54094864-54094865	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:101)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
Gastrointestinal stromal cancer	17527083	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17209131	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:54064400-54106600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:54066400-54099000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:54077800-54107600	Weak transcription	Lung	lung
4	chr4:54078000-54107200	Weak transcription	Primary T cells from cord blood	blood
5	chr4:54089800-54098800	Weak transcription	NHDF-Ad	bronchial
6	chr4:54090000-54107200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr4:54092800-54099200	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr4:54093000-54093800	Strong transcription	Primary B cells from cord blood	blood
9	chr4:54093800-54110800	Weak transcription	Primary B cells from cord blood	blood
10	chr4:54094000-54094600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:54094200-54094400	Enhancers	Primary hematopoietic stem cells	blood
12	chr4:54094200-54094600	Enhancers	K562	blood
13	chr4:54094400-54098600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr4:54094400-54106600	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr4:54094600-54098400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:54094600-54103400	Weak transcription	K562	blood
17	chr4:54096800-54104800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr4:54097200-54101000	Weak transcription	Left Ventricle	heart
19	chr4:54097400-54097800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:54097800-54098200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:54098200-54100600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:54098400-54098800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:54098600-54099800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr4:54098600-54100000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr4:54098600-54100200	Enhancers	Primary hematopoietic stem cells	blood
26	chr4:54098800-54099000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:54098800-54099000	Enhancers	NHDF-Ad	bronchial
28	chr4:54098800-54099800	Enhancers	Primary B cells from peripheral blood	blood
29	chr4:54098800-54100000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr4:54098800-54100000	Enhancers	Osteobl	bone
31	chr4:54099000-54099200	Enhancers	Psoas Muscle	Psoas
32	chr4:54099000-54099400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:54099000-54099400	Weak transcription	NHDF-Ad	bronchial
34	chr4:54099000-54099800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr4:54099000-54101200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:54099200-54107200	Weak transcription	Psoas Muscle	Psoas
37	chr4:54099400-54099600	Enhancers	NHDF-Ad	bronchial
38	chr4:54099400-54099600	Enhancers	NHEK	skin
39	chr4:54099400-54099800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:54099400-54099800	Enhancers	Ovary	ovary
41	chr4:54099400-54100400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:54099600-54099800	Enhancers	GM12878-XiMat	blood
43	chr4:54099600-54100000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr4:54099600-54100200	Weak transcription	NHEK	skin
45	chr4:54099600-54106600	Weak transcription	NHDF-Ad	bronchial
46	chr4:54099800-54100800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:54099800-54100800	Weak transcription	GM12878-XiMat	blood
48	chr4:54099800-54101200	Weak transcription	Primary B cells from peripheral blood	blood
49	chr4:54099800-54102400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr4:54099800-54107200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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