Variant report

Variant	esv2763360
Chromosome Location	chr4:54123894-54153814
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:56)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:56 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:54147733-54148049	HepG2	liver:	n/a	chr4:54147875-54147886 chr4:54147875-54147888
2	CEBPB	chr4:54131944-54132027	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr4:54147714-54148053	IMR90	lung:	n/a	chr4:54147875-54147886 chr4:54147875-54147888
4	CEBPB	chr4:54147739-54148039	K562	blood:	n/a	chr4:54147875-54147886 chr4:54147875-54147888
5	CTCF	chr4:54153034-54153138	MCF-7	breast:	n/a	n/a
6	CTCF	chr4:54129840-54129990	BE2_C	brain:	n/a	n/a
7	CTCF	chr4:54129813-54129978	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr4:54129872-54129886	MCF-7	breast:	n/a	n/a
9	CTCF	chr4:54129897-54129935	MCF-7	breast:	n/a	n/a
10	CTCF	chr4:54152994-54153139	Fibrobl	skin:	n/a	n/a
11	CTCF	chr4:54134857-54134909	Fibrobl	skin:	n/a	n/a
12	CTCF	chr4:54125992-54126037	GM13976	blood:	n/a	n/a
13	CTCF	chr4:54129820-54129970	GM12864	blood:	n/a	n/a
14	CTCF	chr4:54129860-54130010	HepG2	liver:	n/a	n/a
15	CTCF	chr4:54153061-54153124	MCF-7	breast:	n/a	n/a
16	CTCF	chr4:54129784-54129895	GM10248	blood:	n/a	n/a
17	CTCF	chr4:54129125-54129217	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr4:54153014-54153134	MCF-7	breast:	n/a	n/a
19	CTCF	chr4:54153052-54153114	MCF-7	breast:	n/a	n/a
20	CTCF	chr4:54129880-54129903	GM19240	blood:	n/a	n/a
21	CTCF	chr4:54153035-54153161	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:54129868-54129875	GM19240	blood:	n/a	n/a
23	CTCF	chr4:54129930-54129983	GM20000	blood:	n/a	n/a
24	CTCF	chr4:54129906-54129914	GM19240	blood:	n/a	n/a
25	E2F4	chr4:54145113-54145302	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr4:54136701-54136815	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr4:54140005-54140267	MCF10A-Er-Src	breast:	n/a	n/a
28	GATA2	chr4:54124089-54124335	HUVEC	blood vessel:	n/a	chr4:54124126-54124134 chr4:54124194-54124203 chr4:54124189-54124203
29	MAFK	chr4:54146703-54146899	HepG2	liver:	n/a	n/a
30	MAFK	chr4:54144680-54144880	HepG2	liver:	n/a	chr4:54144723-54144738 chr4:54144727-54144738 chr4:54144726-54144740
31	MAFK	chr4:54144616-54144807	HepG2	liver:	n/a	chr4:54144723-54144738 chr4:54144727-54144738 chr4:54144726-54144740
32	PAX5	chr4:54145819-54145986	GM12878	blood:	n/a	n/a
33	POLR2A	chr4:54129025-54129150	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr4:54149407-54149504	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr4:54142422-54142477	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr4:54137848-54137942	ProgFib	skin:	n/a	n/a
37	POLR2A	chr4:54152818-54152891	Gliobla	brain:	n/a	n/a
38	POLR2A	chr4:54133231-54133352	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr4:54153388-54153469	Gliobla	brain:	n/a	n/a
40	POLR2A	chr4:54152750-54152793	Gliobla	brain:	n/a	n/a
41	POLR2A	chr4:54130345-54130446	Gliobla	brain:	n/a	n/a
42	POLR2A	chr4:54146054-54146102	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr4:54130448-54130477	Gliobla	brain:	n/a	n/a
44	POLR2A	chr4:54130486-54130511	Gliobla	brain:	n/a	n/a
45	POLR2A	chr4:54137484-54137543	MCF10A-Er-Src	breast:	n/a	n/a
46	RAD21	chr4:54129802-54130100	H1-hESC	embryonic stem cell:	n/a	n/a
47	RAD21	chr4:54129851-54129953	H1-hESC	embryonic stem cell:	n/a	n/a
48	RUNX3	chr4:54142887-54143164	GM12878	blood:	n/a	n/a
49	STAT3	chr4:54140081-54140234	MCF10A-Er-Src	breast:	n/a	chr4:54140201-54140209
50	STAT3	chr4:54147996-54148028	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:54152475-54152525	Hela-S3	cervix:	n/a
2	chr4:54152475-54152525	IMR90	lung:	fetal
3	chr4:54152475-54152525	ovcar-3	ovarian:	n/a
4	chr4:54152475-54152525	HNPCEpiC	eye:	n/a
5	chr4:54152475-54152525	HepG2	liver:	n/a
6	chr4:54152475-54152525	HCM	heart:	n/a
7	chr4:54152475-54152525	PANC-1	pancreas:	n/a
8	chr4:54152475-54152525	GM12878	blood:	n/a
9	chr4:54152475-54152525	NH-A	brain:	n/a
10	chr4:54152475-54152525	K562	blood:	n/a
11	chr4:54152475-54152525	U87	brain:	n/a
12	chr4:54152475-54152525	CMK	blood:	n/a
13	chr4:54152475-54152525	BE2_C	brain:	n/a
14	chr4:54152475-54152525	MCF-7	breast:	n/a
15	chr4:54152475-54152525	HUVEC	blood vessel:	n/a
16	chr4:54152475-54152525	Caco-2	colon:	n/a
17	chr4:54152475-54152525	AoSMC	blood vessel:	n/a
18	chr4:54152475-54152525	AG09319	gingival:	n/a
19	chr4:54152475-54152525	PrEC	prostate:	n/a
20	chr4:54152475-54152525	PFSK-1	brain:	n/a
21	chr4:54152475-54152525	HCT-116	colon:	n/a
22	chr4:54152475-54152525	MCF10A-Er-Src	breast:	n/a
23	chr4:54152475-54152525	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:54152475-54152525	GM06990	blood:	n/a
25	chr4:54152475-54152525	HCF	heart:	n/a
26	chr4:54152475-54152525	SKMC	muscle:	n/a
27	chr4:54152475-54152525	Jurkat	blood:	n/a
28	chr4:54152475-54152525	SAEC	small airway:	n/a
29	chr4:54152475-54152525	GM12892	blood:	n/a
30	chr4:54152475-54152525	AG04449	skin:	fetal
31	chr4:54152475-54152525	H1-hESC	embryonic stem cell:	embryo
32	chr4:54152475-54152525	SK-N-SH	brain:	n/a
33	chr4:54152475-54152525	NHDF-neo	bronchial:	n/a
34	chr4:54152475-54152525	LNCaP	prostate:	n/a
35	chr4:54152475-54152525	HAEpiC	amniotic membrane:	n/a
36	chr4:54152475-54152525	HRE	kidney:	n/a
37	chr4:54152475-54152525	HIPEpiC	eye:	n/a
38	chr4:54152475-54152525	ProgFib	skin:	n/a
39	chr4:54152475-54152525	HMEC	breast:	n/a
40	chr4:54152475-54152525	RPTEC	kidney:	n/a
41	chr4:54152475-54152525	AG04450	lung:	fetal
42	chr4:54152475-54152525	ECC-1	luminal epithelium:	n/a
43	chr4:54152475-54152525	Hepatocyte	liver:	n/a
44	chr4:54152475-54152525	A549	lung:	n/a
45	chr4:54152475-54152525	NB4	blood:	n/a
46	chr4:54152475-54152525	AG09309	skin:	n/a
47	chr4:54152475-54152525	AG10803	skin:	n/a
48	chr4:54152475-54152525	HEK293	kidney:	embryo
49	chr4:54152475-54152525	BJ	skin:	n/a
50	chr4:54152475-54152525	HEEpiC	esophagus:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:54149656..54152497-chr4:54155266..54158349,3	K562	blood:
2	chr4:54124166..54126954-chr4:54482299..54484673,2	K562	blood:
3	chr4:54107331..54109180-chr4:54137571..54139298,2	K562	blood:
4	chr4:54150463..54153230-chr4:54155569..54157322,2	MCF-7	breast:
5	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
ENSG00000207385	chromatin interactions
ENSG00000072201	chromatin interactions

Extended variants
information (count: 1046 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538657110	chr4:54123902-54123903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187036009	chr4:54123903-54123904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558617354	chr4:54123912-54123913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35537981	chr4:54123949-54123950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371883955	chr4:54123951-54123952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570785916	chr4:54123955-54123956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532911437	chr4:54124028-54124029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549524544	chr4:54124040-54124041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569082541	chr4:54124041-54124042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs578245010	chr4:54124059-54124060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569688545	chr4:54124109-54124110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375193989	chr4:54124119-54124120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190178738	chr4:54124121-54124122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555085852	chr4:54124155-54124156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570399713	chr4:54124156-54124157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565921565	chr4:54124160-54124161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75887007	chr4:54124171-54124172	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs534534474	chr4:54124204-54124205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs558003019	chr4:54124283-54124284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs578198959	chr4:54124355-54124356	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554060916	chr4:54124500-54124501	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543759991	chr4:54124533-54124534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs138170421	chr4:54124543-54124544	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs574025556	chr4:54124566-54124567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs367943740	chr4:54124567-54124568	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188639494	chr4:54124569-54124570	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs143746004	chr4:54124583-54124584	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527458863	chr4:54124599-54124600	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs114610616	chr4:54124655-54124656	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs193138305	chr4:54124669-54124670	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs564335763	chr4:54124674-54124675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs556230952	chr4:54124686-54124687	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs574564192	chr4:54124687-54124688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs201888049	chr4:54124696-54124697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372669406	chr4:54124706-54124707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs13128531	chr4:54124707-54124708	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550099019	chr4:54124710-54124711	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs71197011	chr4:54124730-54124731	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs59321045	chr4:54124732-54124733	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7683382	chr4:54124744-54124745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372117787	chr4:54124748-54124749	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373583308	chr4:54124750-54124751	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs74468078	chr4:54124761-54124762	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs191155233	chr4:54124782-54124783	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs183581998	chr4:54124819-54124820	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs534856445	chr4:54124914-54124915	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs553968717	chr4:54124933-54124934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs557939873	chr4:54124971-54124972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs199729604	chr4:54124973-54124974	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112016184	chr4:54124979-54124980	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

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:190 , 50 per page) page: 1 2 3 4

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	chr4:54114600-54126400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr4:54114600-54129800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:54114800-54129400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:54114800-54130000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr4:54117800-54132800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:54119600-54130400	Weak transcription	NHLF	lung
12	chr4:54120600-54124000	Weak transcription	Primary T cells from cord blood	blood
13	chr4:54122200-54139800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr4:54122600-54127400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr4:54126400-54126600	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
16	chr4:54126600-54126800	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr4:54126600-54134200	Weak transcription	Gastric	stomach
18	chr4:54126800-54141400	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr4:54127200-54130200	Weak transcription	Primary hematopoietic stem cells	blood
20	chr4:54127400-54127600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr4:54127600-54153000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr4:54128000-54129600	Weak transcription	HSMMtube	muscle
23	chr4:54128000-54134400	Weak transcription	Pancreas	Pancrea
24	chr4:54128200-54136200	Weak transcription	Thymus	Thymus
25	chr4:54128600-54128800	Weak transcription	Fetal Lung	lung
26	chr4:54128600-54132800	Weak transcription	Adipose Nuclei	Adipose
27	chr4:54129400-54130000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:54129400-54130800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:54129400-54130800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr4:54129600-54130400	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
31	chr4:54129600-54130400	Strong transcription	HSMMtube	muscle
32	chr4:54129600-54130600	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr4:54129600-54130800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr4:54129600-54141400	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr4:54129600-54154600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr4:54129800-54130200	ZNF genes & repeats	Fetal Muscle Trunk	muscle
37	chr4:54129800-54130400	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
38	chr4:54129800-54130600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr4:54129800-54130600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr4:54129800-54130600	ZNF genes & repeats	Fetal Stomach	stomach
41	chr4:54129800-54130800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
42	chr4:54129800-54145200	Weak transcription	Fetal Lung	lung
43	chr4:54130000-54130200	Weak transcription	Primary B cells from peripheral blood	blood
44	chr4:54130000-54130400	ZNF genes & repeats	Primary T cells from cord blood	blood
45	chr4:54130000-54130600	Strong transcription	Duodenum Mucosa	Duodenum
46	chr4:54130000-54130600	ZNF genes & repeats	Dnd41	blood
47	chr4:54130000-54134600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr4:54130000-54135800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr4:54130200-54130400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
50	chr4:54130200-54130400	Strong transcription	Fetal Muscle Trunk	muscle

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