Variant report

Variant	nsv1008593
Chromosome Location	chr4:54120297-54207769
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:246)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:54188755-54189327	HepG2	liver:	n/a	n/a
2	BACH1	chr4:54187548-54187991	H1-hESC	embryonic stem cell:	n/a	chr4:54187775-54187789
3	BATF	chr4:54174085-54174339	GM12878	blood:	n/a	n/a
4	BATF	chr4:54192769-54192979	GM12878	blood:	n/a	n/a
5	BATF	chr4:54175943-54176126	GM12878	blood:	n/a	chr4:54176008-54176019
6	CEBPB	chr4:54171521-54171615	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:54147733-54148049	HepG2	liver:	n/a	chr4:54147875-54147886 chr4:54147875-54147888
8	CEBPB	chr4:54131944-54132027	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:54147714-54148053	IMR90	lung:	n/a	chr4:54147875-54147886 chr4:54147875-54147888
10	CEBPB	chr4:54187220-54187904	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:54147739-54148039	K562	blood:	n/a	chr4:54147875-54147886 chr4:54147875-54147888
12	CEBPB	chr4:54187233-54187859	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:54156497-54156697	K562	blood:	n/a	n/a
14	CEBPB	chr4:54187233-54187808	HCT-116	colon:	n/a	n/a
15	CEBPB	chr4:54187262-54187626	ECC-1	luminal epithelium:	n/a	n/a
16	CTCF	chr4:54179812-54179893	GM12878	blood:	n/a	n/a
17	CTCF	chr4:54206795-54206981	Gliobla	brain:	n/a	n/a
18	CTCF	chr4:54206800-54206950	K562	blood:	n/a	n/a
19	CTCF	chr4:54179705-54179982	MCF-7	breast:	n/a	n/a
20	CTCF	chr4:54179770-54179906	A549	lung:	n/a	n/a
21	CTCF	chr4:54179659-54179962	A549	lung:	n/a	n/a
22	CTCF	chr4:54206800-54206950	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr4:54206760-54206910	HCT-116	colon:	n/a	n/a
24	CTCF	chr4:54179800-54179950	HMF	breast:	n/a	n/a
25	CTCF	chr4:54179582-54180127	HCT-116	colon:	n/a	n/a
26	CTCF	chr4:54179708-54179957	Gliobla	brain:	n/a	n/a
27	CTCF	chr4:54190640-54190790	HepG2	liver:	n/a	n/a
28	CTCF	chr4:54179700-54179850	NHDF-neo	bronchial:	n/a	n/a
29	CTCF	chr4:54179752-54179901	T-47D	breast:	n/a	n/a
30	CTCF	chr4:54179719-54179956	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:54129880-54129903	GM19240	blood:	n/a	n/a
32	CTCF	chr4:54179780-54179930	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr4:54179740-54179890	HCM	heart:	n/a	n/a
34	CTCF	chr4:54206804-54206935	ProgFib	skin:	n/a	n/a
35	CTCF	chr4:54179780-54179930	AG04450	lung:	n/a	n/a
36	CTCF	chr4:54179780-54179930	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr4:54129820-54129970	GM12864	blood:	n/a	n/a
38	CTCF	chr4:54179760-54179910	GM12873	blood:	n/a	n/a
39	CTCF	chr4:54206800-54206950	HEK293	kidney:	n/a	n/a
40	CTCF	chr4:54153014-54153134	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:54134857-54134909	Fibrobl	skin:	n/a	n/a
42	CTCF	chr4:54179723-54179922	ProgFib	skin:	n/a	n/a
43	CTCF	chr4:54190680-54190830	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr4:54179802-54179864	GM19238	blood:	n/a	n/a
45	CTCF	chr4:54179760-54179910	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr4:54153061-54153124	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:54179740-54179890	WI-38	lung:	n/a	n/a
48	CTCF	chr4:54179749-54179938	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr4:54179800-54179904	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr4:54179840-54179990	AG09319	gingival:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:54187654-54187704	SK-N-SH_RA	brain:	n/a
2	chr4:54195199-54195249	Jurkat	blood:	n/a
3	chr4:54187654-54187704	SK-N-SH_RA	brain:	n/a
4	chr4:54195199-54195249	Jurkat	blood:	n/a
5	chr4:54152475-54152525	PrEC	prostate:	n/a
6	chr4:54187654-54187704	ovcar-3	ovarian:	n/a
7	chr4:54173521-54173571	PFSK-1	brain:	n/a
8	chr4:54187654-54187704	MCF10A-Er-Src	breast:	n/a
9	chr4:54195199-54195249	SK-N-SH	brain:	n/a
10	chr4:54152475-54152525	NB4	blood:	n/a
11	chr4:54187654-54187704	AG09309	skin:	n/a
12	chr4:54195199-54195249	BE2_C	brain:	n/a
13	chr4:54173521-54173571	NT2-D1	testis:	n/a
14	chr4:54173521-54173571	SK-N-SH	brain:	n/a
15	chr4:54173521-54173571	HRCEpiC	kidney:	n/a
16	chr4:54152475-54152525	AG10803	skin:	n/a
17	chr4:54195199-54195249	SKMC	muscle:	n/a
18	chr4:54173521-54173571	GM12878	blood:	n/a
19	chr4:54195199-54195249	T-47D	breast:	n/a
20	chr4:54152475-54152525	HCPEpiC	choroid plexus:	n/a
21	chr4:54152475-54152525	HUVEC	blood vessel:	n/a
22	chr4:54152475-54152525	GM19239	blood:	n/a
23	chr4:54187654-54187704	H1-hESC	embryonic stem cell:	embryo
24	chr4:54152475-54152525	NHDF-neo	bronchial:	n/a
25	chr4:54187654-54187704	PrEC	prostate:	n/a
26	chr4:54173521-54173571	SKMC	muscle:	n/a
27	chr4:54187654-54187704	HNPCEpiC	eye:	n/a
28	chr4:54195199-54195249	SK-N-SH_RA	brain:	n/a
29	chr4:54187654-54187704	HUVEC	blood vessel:	n/a
30	chr4:54152475-54152525	HRE	kidney:	n/a
31	chr4:54195199-54195249	HL-60	blood:	n/a
32	chr4:54152475-54152525	H1-hESC	embryonic stem cell:	embryo
33	chr4:54173521-54173571	ProgFib	skin:	n/a
34	chr4:54152475-54152525	CMK	blood:	n/a
35	chr4:54173521-54173571	HUVEC	blood vessel:	n/a
36	chr4:54187654-54187704	NB4	blood:	n/a
37	chr4:54187654-54187704	AG10803	skin:	n/a
38	chr4:54152475-54152525	IMR90	lung:	fetal
39	chr4:54195199-54195249	HRE	kidney:	n/a
40	chr4:54195199-54195249	CMK	blood:	n/a
41	chr4:54173521-54173571	IMR90	lung:	fetal
42	chr4:54173521-54173571	HCPEpiC	choroid plexus:	n/a
43	chr4:54195199-54195249	HCF	heart:	n/a
44	chr4:54195199-54195249	SK-N-MC	brain:	n/a
45	chr4:54195199-54195249	NT2-D1	testis:	n/a
46	chr4:54152475-54152525	MCF-7	breast:	n/a
47	chr4:54187654-54187704	HIPEpiC	eye:	n/a
48	chr4:54195199-54195249	ECC-1	luminal epithelium:	n/a
49	chr4:54173521-54173571	LNCaP	prostate:	n/a
50	chr4:54173521-54173571	HCT-116	colon:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:54170671..54173423-chr4:54174162..54176514,4	K562	blood:
2	chr4:54181996..54184971-chr4:54188606..54191162,2	K562	blood:
3	chr4:54188711..54191602-chr4:54194336..54196357,3	MCF-7	breast:
4	chr4:54130628..54132899-chr4:54134873..54136531,2	K562	blood:
5	chr4:54187046..54188673-chr4:54816708..54819135,2	K562	blood:
6	chr4:54181996..54184971-chr4:54188606..54191162,2	K562	blood:
7	chr4:54150463..54153230-chr4:54155569..54157322,2	MCF-7	breast:
8	chr4:54179815..54180318-chr4:55099127..55100044,2	MCF-7	breast:
9	chr4:54150463..54153230-chr4:54155569..54157322,2	MCF-7	breast:
10	chr4:54174793..54178568-chr4:54179278..54182842,3	K562	blood:
11	chr4:54187902..54191674-chr4:54240790..54245146,4	K562	blood:
12	chr4:54179624..54180337-chr4:54572546..54573241,2	MCF-7	breast:
13	chr4:54149656..54152497-chr4:54155266..54158349,3	K562	blood:
14	chr4:54174793..54178568-chr4:54179278..54182842,3	K562	blood:
15	chr4:54188711..54191602-chr4:54194336..54196357,3	MCF-7	breast:
16	chr4:54124166..54126954-chr4:54482299..54484673,2	K562	blood:
17	chr4:54170671..54173423-chr4:54174162..54176514,4	K562	blood:
18	chr4:54149656..54152497-chr4:54155266..54158349,3	K562	blood:
19	chr4:54107331..54109180-chr4:54137571..54139298,2	K562	blood:
20	chr4:54189381..54192289-chr4:54225390..54227356,2	K562	blood:
21	chr4:54184058..54186336-chr4:54222411..54224746,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-310P	TF binding region
RNU6-310P	CpG island
ENSG00000207385	chromatin interactions
ENSG00000145216	chromatin interactions
ENSG00000072201	chromatin interactions

Extended variants
information (count: 3356 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3356 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139497600	chr4:54120312-54120313	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs530612419	chr4:54120314-54120315	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs562665435	chr4:54120341-54120342	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs186129722	chr4:54120354-54120355	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs529918667	chr4:54120370-54120371	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs567660583	chr4:54120376-54120377	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs115770218	chr4:54120378-54120379	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs149698645	chr4:54120380-54120381	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs566848441	chr4:54120389-54120390	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs73147392	chr4:54120390-54120391	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs11133257	chr4:54120462-54120463	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs115649865	chr4:54120508-54120509	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs538058217	chr4:54120555-54120556	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs201902552	chr4:54120594-54120595	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs192232340	chr4:54120660-54120661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199750206	chr4:54120704-54120705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571582755	chr4:54120711-54120712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542678988	chr4:54120736-54120737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11133258	chr4:54120746-54120747	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs375738612	chr4:54120805-54120806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143892286	chr4:54120806-54120807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182685059	chr4:54120812-54120813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564836108	chr4:54120822-54120823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146901687	chr4:54120830-54120831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550514388	chr4:54120836-54120837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561105161	chr4:54120869-54120870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530162204	chr4:54120885-54120886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373670008	chr4:54120898-54120899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201695848	chr4:54120913-54120914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551712586	chr4:54120941-54120942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200956052	chr4:54120973-54120974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538971952	chr4:54120977-54120978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367931995	chr4:54120986-54120987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201239297	chr4:54121003-54121004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377088317	chr4:54121013-54121014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202073148	chr4:54121015-54121016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568416284	chr4:54121016-54121017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566910123	chr4:54121025-54121026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375734244	chr4:54121027-54121028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71197009	chr4:54121030-54121031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187859005	chr4:54121062-54121063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376070565	chr4:54121070-54121071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539081573	chr4:54121071-54121072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191346183	chr4:54121074-54121075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182530512	chr4:54121100-54121101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564851574	chr4:54121111-54121112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187522587	chr4:54121141-54121142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192039526	chr4:54121149-54121150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535998278	chr4:54121156-54121157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552642787	chr4:54121191-54121192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Glioblastoma multiforme	21138945	CNVD
Cancer	17440070	CNVD

Chromatin state (count:745 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:54101600-54129400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:54108400-54129600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:54114400-54134400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:54114400-54139600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:54114400-54144000	Weak transcription	Liver	Liver
6	chr4:54114600-54121000	Weak transcription	Pancreas	Pancrea
7	chr4:54114600-54126400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr4:54114600-54129800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr4:54114800-54129400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:54114800-54130000	Weak transcription	Duodenum Mucosa	Duodenum
11	chr4:54116400-54120400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr4:54117800-54132800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:54119600-54130400	Weak transcription	NHLF	lung
14	chr4:54120000-54120400	Weak transcription	Fetal Stomach	stomach
15	chr4:54120200-54120600	ZNF genes & repeats	Fetal Lung	lung
16	chr4:54120400-54120600	ZNF genes & repeats	Primary T cells from cord blood	blood
17	chr4:54120400-54120600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:54120400-54120600	ZNF genes & repeats	Fetal Stomach	stomach
19	chr4:54120600-54121600	Weak transcription	Fetal Lung	lung
20	chr4:54120600-54123200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:54120600-54124000	Weak transcription	Primary T cells from cord blood	blood
22	chr4:54122200-54139800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr4:54122600-54127400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr4:54122800-54123200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr4:54123200-54123600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
26	chr4:54123200-54123600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:54126400-54126600	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
28	chr4:54126600-54126800	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr4:54126600-54134200	Weak transcription	Gastric	stomach
30	chr4:54126800-54141400	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr4:54127200-54130200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr4:54127400-54127600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr4:54127600-54153000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr4:54128000-54129600	Weak transcription	HSMMtube	muscle
35	chr4:54128000-54134400	Weak transcription	Pancreas	Pancrea
36	chr4:54128200-54136200	Weak transcription	Thymus	Thymus
37	chr4:54128600-54128800	Weak transcription	Fetal Lung	lung
38	chr4:54128600-54132800	Weak transcription	Adipose Nuclei	Adipose
39	chr4:54129400-54130000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:54129400-54130800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr4:54129400-54130800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr4:54129600-54130400	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
43	chr4:54129600-54130400	Strong transcription	HSMMtube	muscle
44	chr4:54129600-54130600	ZNF genes & repeats	Fetal Intestine Small	intestine
45	chr4:54129600-54130800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr4:54129600-54141400	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr4:54129600-54154600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr4:54129800-54130200	ZNF genes & repeats	Fetal Muscle Trunk	muscle
49	chr4:54129800-54130400	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
50	chr4:54129800-54130600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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