Variant report

Variant	nsv1032446
Chromosome Location	chr7:57855343-58019983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1665)
CpG islands
(count:915)
Chromatin interactive
region (count:0)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1665 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:58010298-58010461	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:57994141-57994509	HepG2	liver:	n/a	n/a
3	ATF1	chr7:57960924-57961116	K562	blood:	n/a	n/a
4	ATF1	chr7:57981808-57982008	K562	blood:	n/a	n/a
5	ATF1	chr7:57995641-57996010	K562	blood:	n/a	n/a
6	ATF1	chr7:57994002-57994510	K562	blood:	n/a	n/a
7	BACH1	chr7:57973523-57973897	K562	blood:	n/a	n/a
8	BACH1	chr7:58012973-58012998	K562	blood:	n/a	n/a
9	BACH1	chr7:57953074-57953078	K562	blood:	n/a	n/a
10	BACH1	chr7:58012803-58012998	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:57995639-57996394	K562	blood:	n/a	n/a
12	BACH1	chr7:57965177-57965554	K562	blood:	n/a	n/a
13	BATF	chr7:57940526-57940743	GM12878	blood:	n/a	n/a
14	BATF	chr7:57999505-57999877	GM12878	blood:	n/a	n/a
15	BATF	chr7:58006674-58006965	GM12878	blood:	n/a	n/a
16	BATF	chr7:57961728-57962181	GM12878	blood:	n/a	n/a
17	BATF	chr7:57984864-57985086	GM12878	blood:	n/a	n/a
18	BATF	chr7:57992052-57992285	GM12878	blood:	n/a	n/a
19	BATF	chr7:57957699-57958079	GM12878	blood:	n/a	n/a
20	BATF	chr7:58009212-58009591	GM12878	blood:	n/a	n/a
21	BATF	chr7:57956471-57956682	GM12878	blood:	n/a	n/a
22	BATF	chr7:57999368-57999788	GM12878	blood:	n/a	n/a
23	BATF	chr7:58014452-58014715	GM12878	blood:	n/a	n/a
24	BATF	chr7:58008446-58008790	GM12878	blood:	n/a	n/a
25	BATF	chr7:58007790-58008139	GM12878	blood:	n/a	n/a
26	BATF	chr7:58013747-58014011	GM12878	blood:	n/a	n/a
27	BATF	chr7:57994043-57994353	GM12878	blood:	n/a	n/a
28	BATF	chr7:57924008-57924207	GM12878	blood:	n/a	chr7:57924188-57924197
29	BATF	chr7:57940500-57940831	GM12878	blood:	n/a	n/a
30	BATF	chr7:57984879-57985099	GM12878	blood:	n/a	n/a
31	BATF	chr7:57994669-57994997	GM12878	blood:	n/a	n/a
32	BATF	chr7:58014454-58014600	GM12878	blood:	n/a	n/a
33	BATF	chr7:58009224-58009514	GM12878	blood:	n/a	n/a
34	BATF	chr7:57970948-57971464	GM12878	blood:	n/a	n/a
35	BATF	chr7:57953748-57954008	GM12878	blood:	n/a	n/a
36	BATF	chr7:57978026-57978220	GM12878	blood:	n/a	n/a
37	BATF	chr7:57994095-57994356	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:58014445-58014652	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:57953745-57954012	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:57999427-57999766	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:57957710-57958115	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:58009181-58009601	GM12878	blood:	n/a	n/a
43	BCL11A	chr7:57940416-57940867	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:57953847-57954001	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:58007141-58007414	GM12878	blood:	n/a	n/a
46	BCL11A	chr7:57882040-57882219	GM12878	blood:	n/a	n/a
47	BCL11A	chr7:57983814-57984055	GM12878	blood:	n/a	n/a
48	BCL11A	chr7:57948329-57948539	GM12878	blood:	n/a	n/a
49	BCL11A	chr7:57956472-57956675	GM12878	blood:	n/a	n/a
50	BCL11A	chr7:58014338-58014759	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:57880009-57880059	IMR90	lung:	fetal
2	chr7:57928306-57928356	NHDF-neo	bronchial:	n/a
3	chr7:57880009-57880059	AoSMC	blood vessel:	n/a
4	chr7:57878945-57878995	HRPEpiC	eye:	n/a
5	chr7:57895070-57895120	HIPEpiC	eye:	n/a
6	chr7:57927758-57927808	HMEC	breast:	n/a
7	chr7:57880009-57880059	BE2_C	brain:	n/a
8	chr7:57924074-57924124	MCF-7	breast:	n/a
9	chr7:57881100-57881150	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:57881130-57881180	SK-N-SH	brain:	n/a
11	chr7:57928306-57928356	HAEpiC	amniotic membrane:	n/a
12	chr7:57895070-57895120	BJ	skin:	n/a
13	chr7:57930428-57930478	GM19239	blood:	n/a
14	chr7:57928998-57929048	HRE	kidney:	n/a
15	chr7:57895070-57895120	CMK	blood:	n/a
16	chr7:57878777-57878827	MCF-7	breast:	n/a
17	chr7:57881100-57881150	SKMC	muscle:	n/a
18	chr7:57880009-57880059	HIPEpiC	eye:	n/a
19	chr7:57927783-57927833	ECC-1	luminal epithelium:	n/a
20	chr7:57928306-57928356	LNCaP	prostate:	n/a
21	chr7:57896675-57896725	SKMC	muscle:	n/a
22	chr7:57927758-57927808	GM19239	blood:	n/a
23	chr7:57881130-57881180	GM06990	blood:	n/a
24	chr7:57927793-57927843	PANC-1	pancreas:	n/a
25	chr7:57928306-57928356	PrEC	prostate:	n/a
26	chr7:57896675-57896725	SK-N-SH_RA	brain:	n/a
27	chr7:57895070-57895120	HRCEpiC	kidney:	n/a
28	chr7:57880009-57880059	MCF10A-Er-Src	breast:	n/a
29	chr7:57895070-57895120	RPTEC	kidney:	n/a
30	chr7:57924074-57924124	SK-N-SH	brain:	n/a
31	chr7:57928306-57928356	CMK	blood:	n/a
32	chr7:57928998-57929048	HRPEpiC	eye:	n/a
33	chr7:57878945-57878995	PANC-1	pancreas:	n/a
34	chr7:57878777-57878827	HMEC	breast:	n/a
35	chr7:57880009-57880059	AG04449	skin:	fetal
36	chr7:57927783-57927833	GM12891	blood:	n/a
37	chr7:57927783-57927833	PFSK-1	brain:	n/a
38	chr7:57878945-57878995	Hepatocyte	liver:	n/a
39	chr7:57878945-57878995	HIPEpiC	eye:	n/a
40	chr7:57878945-57878995	GM19239	blood:	n/a
41	chr7:57927758-57927808	AG04449	skin:	fetal
42	chr7:57924074-57924124	HNPCEpiC	eye:	n/a
43	chr7:57928998-57929048	BJ	skin:	n/a
44	chr7:57927783-57927833	SK-N-SH_RA	brain:	n/a
45	chr7:57878945-57878995	HepG2	liver:	n/a
46	chr7:57896675-57896725	HIPEpiC	eye:	n/a
47	chr7:57878777-57878827	K562	blood:	n/a
48	chr7:57927758-57927808	HEK293	kidney:	embryo
49	chr7:57878777-57878827	ProgFib	skin:	n/a
50	chr7:57924074-57924124	SKMC	muscle:	n/a

No data

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF716-24	chr7:57896673-57896752	NONHSAT120882
2	lnc-ZNF716-24	chr7:57894964-57895190	NONHSAT120882
3	lnc-ZNF716-24	chr7:57888037-57888136	NONHSAT120882
4	lnc-ZNF479-16	chr7:57882150-57882506	NONHSAT120880
5	lnc-ZNF479-15	chr7:57879738-57880116	NONHSAT120878
6	lnc-ZNF479-14	chr7:57877307-57877718	NONHSAT120873

No data

Variant related genes	Relation type
ENSG00000224653	TF binding region
ENSG00000231484	TF binding region
ENSG00000231232	TF binding region
ENSG00000237236	TF binding region
ENSG00000236907	TF binding region
ENSG00000271696	TF binding region
ENSG00000250618	TF binding region
ENSG00000223836	TF binding region
ENSG00000224653	CpG island
ENSG00000231484	CpG island
ENSG00000231232	CpG island
ENSG00000237236	CpG island
ENSG00000236907	CpG island
ENSG00000271696	CpG island
ENSG00000250618	CpG island
ENSG00000223836	CpG island

Extended variants
information (count: 12413 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:12413 , 50 per page) page: 1 2 3 4 5 6 7 ... 249

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200390592	chr7:57876314-57876315	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs200911623	chr7:57876333-57876334	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs372719745	chr7:57876598-57876599	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs143360676	chr7:57877322-57877323	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs562656698	chr7:57877328-57877329	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs558427748	chr7:57877350-57877351	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs373230968	chr7:57877367-57877368	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs187511280	chr7:57877368-57877369	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs201593880	chr7:57877410-57877411	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs549490501	chr7:57877437-57877438	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs113814388	chr7:57877439-57877440	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs561344561	chr7:57877440-57877441	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs114954280	chr7:57877446-57877447	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs547296332	chr7:57877465-57877466	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs207467957	chr7:57877469-57877470	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs148356312	chr7:57877478-57877479	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs6557591	chr7:57877485-57877486	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs192726477	chr7:57877515-57877516	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs200563256	chr7:57877516-57877517	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs112156731	chr7:57877523-57877524	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs554324536	chr7:57877592-57877593	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs538499265	chr7:57877599-57877600	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs368910585	chr7:57877610-57877611	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
24	rs7385323	chr7:57877613-57877614	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
25	rs558829857	chr7:57877623-57877624	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
26	rs150538599	chr7:57877636-57877637	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
27	rs572988247	chr7:57877642-57877643	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
28	rs544495481	chr7:57877660-57877661	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
29	rs183218028	chr7:57877662-57877663	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
30	rs7385327	chr7:57877665-57877666	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
31	rs562586101	chr7:57877686-57877687	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
32	rs140248086	chr7:57877688-57877689	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
33	rs561865634	chr7:57877700-57877701	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
34	rs142722019	chr7:57877724-57877725	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs544557038	chr7:57877739-57877740	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs528505108	chr7:57877740-57877741	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs147427943	chr7:57877801-57877802	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs564389852	chr7:57877804-57877805	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs187876848	chr7:57877819-57877820	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs199735422	chr7:57877845-57877846	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs550851287	chr7:57877850-57877851	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs73697621	chr7:57877872-57877873	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs535081777	chr7:57877882-57877883	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs116218620	chr7:57877933-57877934	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs7385065	chr7:57877934-57877935	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs566411070	chr7:57877937-57877938	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs533870165	chr7:57877942-57877943	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs546993489	chr7:57877961-57877962	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs192652297	chr7:57877969-57877970	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs576903675	chr7:57877984-57877985	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Wilms tumour	21544195	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:604 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:57877600-57883400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:57878000-57880000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:57879400-57879600	Enhancers	K562	blood
4	chr7:57879400-57881000	ZNF genes & repeats	Gastric	stomach
5	chr7:57879600-57880800	Weak transcription	K562	blood
6	chr7:57880400-57881400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
7	chr7:57880800-57881200	Enhancers	K562	blood
8	chr7:57880800-57881400	ZNF genes & repeats	Spleen	Spleen
9	chr7:57881200-57881600	Active TSS	K562	blood
10	chr7:57885400-57885800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr7:57885400-57886600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
12	chr7:57885400-57886600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:57885400-57886800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr7:57885800-57886800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
15	chr7:57886000-57886400	ZNF genes & repeats	Esophagus	oesophagus
16	chr7:57886000-57886400	ZNF genes & repeats	Pancreas	Pancrea
17	chr7:57886000-57886600	ZNF genes & repeats	Gastric	stomach
18	chr7:57886000-57886800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:57886200-57886800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:57917400-57918000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr7:57917800-57918400	Active TSS	Fetal Heart	heart
22	chr7:57918200-57918400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
23	chr7:57918200-57918800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
24	chr7:57925000-57925400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
25	chr7:57925400-57927000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr7:57927000-57927200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
27	chr7:57927000-57927600	Active TSS	Liver	Liver
28	chr7:57927000-57927800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
29	chr7:57927000-57928200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr7:57927400-57927800	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
31	chr7:57927400-57929200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:57927600-57927800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
33	chr7:57927600-57927800	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr7:57927600-57927800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:57927600-57927800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:57927600-57927800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr7:57927600-57927800	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
38	chr7:57927600-57927800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
39	chr7:57927600-57927800	Flanking Bivalent TSS/Enh	Liver	Liver
40	chr7:57927600-57927800	Bivalent/Poised TSS	Brain Anterior Caudate	brain
41	chr7:57927600-57927800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
42	chr7:57927600-57927800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr7:57927600-57927800	Bivalent/Poised TSS	Left Ventricle	heart
44	chr7:57927600-57927800	Bivalent/Poised TSS	Right Atrium	heart
45	chr7:57927600-57927800	Bivalent/Poised TSS	Right Ventricle	heart
46	chr7:57927600-57927800	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
47	chr7:57927600-57928000	Bivalent/Poised TSS	Aorta	Aorta
48	chr7:57927600-57928000	Bivalent/Poised TSS	Monocytes-CD14+_RO01746	blood
49	chr7:57927600-57928200	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
50	chr7:57927600-57928200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin

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