Variant report

Variant	nsv1029423
Chromosome Location	chr7:57885902-58019983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1602)
CpG islands
(count:549)
Chromatin interactive
region (count:0)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1602 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

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	chr7:57995641-57996010	K562	blood:	n/a	n/a
5	ATF1	chr7:57994002-57994510	K562	blood:	n/a	n/a
6	ATF1	chr7:57981808-57982008	K562	blood:	n/a	n/a
7	BACH1	chr7:57965177-57965554	K562	blood:	n/a	n/a
8	BACH1	chr7:57995639-57996394	K562	blood:	n/a	n/a
9	BACH1	chr7:57973523-57973897	K562	blood:	n/a	n/a
10	BACH1	chr7:58012973-58012998	K562	blood:	n/a	n/a
11	BACH1	chr7:58012803-58012998	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:57953074-57953078	K562	blood:	n/a	n/a
13	BATF	chr7:57999505-57999877	GM12878	blood:	n/a	n/a
14	BATF	chr7:57940526-57940743	GM12878	blood:	n/a	n/a
15	BATF	chr7:57999368-57999788	GM12878	blood:	n/a	n/a
16	BATF	chr7:58009212-58009591	GM12878	blood:	n/a	n/a
17	BATF	chr7:57970948-57971464	GM12878	blood:	n/a	n/a
18	BATF	chr7:58007790-58008139	GM12878	blood:	n/a	n/a
19	BATF	chr7:57956471-57956682	GM12878	blood:	n/a	n/a
20	BATF	chr7:57992052-57992285	GM12878	blood:	n/a	n/a
21	BATF	chr7:58008446-58008790	GM12878	blood:	n/a	n/a
22	BATF	chr7:57984879-57985099	GM12878	blood:	n/a	n/a
23	BATF	chr7:57994095-57994356	GM12878	blood:	n/a	n/a
24	BATF	chr7:57984864-57985086	GM12878	blood:	n/a	n/a
25	BATF	chr7:57953748-57954008	GM12878	blood:	n/a	n/a
26	BATF	chr7:57924008-57924207	GM12878	blood:	n/a	chr7:57924188-57924197
27	BATF	chr7:57978026-57978220	GM12878	blood:	n/a	n/a
28	BATF	chr7:57994669-57994997	GM12878	blood:	n/a	n/a
29	BATF	chr7:58013747-58014011	GM12878	blood:	n/a	n/a
30	BATF	chr7:57957699-57958079	GM12878	blood:	n/a	n/a
31	BATF	chr7:58014452-58014715	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	chr7:57940500-57940831	GM12878	blood:	n/a	n/a
35	BATF	chr7:58006674-58006965	GM12878	blood:	n/a	n/a
36	BATF	chr7:57961728-57962181	GM12878	blood:	n/a	n/a
37	BATF	chr7:57994043-57994353	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:58009268-58009584	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:57978387-57978589	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:57940500-57940743	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:57981694-57982016	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:57994658-57995145	GM12878	blood:	n/a	n/a
43	BCL11A	chr7:57999330-57999887	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:57953847-57954001	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:57956484-57956699	GM12878	blood:	n/a	n/a
46	BCL11A	chr7:57918662-57918918	GM12878	blood:	n/a	n/a
47	BCL11A	chr7:57983903-57984076	GM12878	blood:	n/a	n/a
48	BCL11A	chr7:58014338-58014759	GM12878	blood:	n/a	n/a
49	BCL11A	chr7:57957710-57958115	GM12878	blood:	n/a	n/a
50	BCL11A	chr7:58009181-58009601	GM12878	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:57927783-57927833	SKMC	muscle:	n/a
2	chr7:57927783-57927833	SK-N-MC	brain:	n/a
3	chr7:57930428-57930478	ovcar-3	ovarian:	n/a
4	chr7:57896675-57896725	NHDF-neo	bronchial:	n/a
5	chr7:57895070-57895120	CMK	blood:	n/a
6	chr7:57924074-57924124	PFSK-1	brain:	n/a
7	chr7:57930428-57930478	HUVEC	blood vessel:	n/a
8	chr7:57895070-57895120	AG09319	gingival:	n/a
9	chr7:57896675-57896725	IMR90	lung:	fetal
10	chr7:57927783-57927833	HepG2	liver:	n/a
11	chr7:57924074-57924124	GM12892	blood:	n/a
12	chr7:57927758-57927808	GM19239	blood:	n/a
13	chr7:57896675-57896725	HIPEpiC	eye:	n/a
14	chr7:57928998-57929048	T-47D	breast:	n/a
15	chr7:57927758-57927808	GM12892	blood:	n/a
16	chr7:57927793-57927843	NH-A	brain:	n/a
17	chr7:57924074-57924124	HCF	heart:	n/a
18	chr7:57928998-57929048	LNCaP	prostate:	n/a
19	chr7:57927783-57927833	RPTEC	kidney:	n/a
20	chr7:57930428-57930478	HRCEpiC	kidney:	n/a
21	chr7:57928306-57928356	ECC-1	luminal epithelium:	n/a
22	chr7:57928306-57928356	Jurkat	blood:	n/a
23	chr7:57927758-57927808	BE2_C	brain:	n/a
24	chr7:57927793-57927843	HRCEpiC	kidney:	n/a
25	chr7:57895070-57895120	HEK293	kidney:	embryo
26	chr7:57896675-57896725	HEK293	kidney:	embryo
27	chr7:57927793-57927843	HRE	kidney:	n/a
28	chr7:57928306-57928356	AG09319	gingival:	n/a
29	chr7:57896675-57896725	HL-60	blood:	n/a
30	chr7:57928306-57928356	PANC-1	pancreas:	n/a
31	chr7:57896675-57896725	SK-N-SH	brain:	n/a
32	chr7:57927758-57927808	NH-A	brain:	n/a
33	chr7:57896675-57896725	NB4	blood:	n/a
34	chr7:57924074-57924124	HRCEpiC	kidney:	n/a
35	chr7:57927758-57927808	HPAEpiC	pulmonary alveolar:	n/a
36	chr7:57930428-57930478	PrEC	prostate:	n/a
37	chr7:57927783-57927833	GM19239	blood:	n/a
38	chr7:57924074-57924124	AG04449	skin:	fetal
39	chr7:57896675-57896725	HCPEpiC	choroid plexus:	n/a
40	chr7:57928998-57929048	AG09319	gingival:	n/a
41	chr7:57896675-57896725	Caco-2	colon:	n/a
42	chr7:57928306-57928356	U87	brain:	n/a
43	chr7:57928306-57928356	SK-N-SH_RA	brain:	n/a
44	chr7:57927758-57927808	AG09319	gingival:	n/a
45	chr7:57928998-57929048	HUVEC	blood vessel:	n/a
46	chr7:57927758-57927808	A549	lung:	n/a
47	chr7:57895070-57895120	T-47D	breast:	n/a
48	chr7:57896675-57896725	PrEC	prostate:	n/a
49	chr7:57927783-57927833	SK-N-SH	brain:	n/a
50	chr7:57930428-57930478	HCM	heart:	n/a

No data

(count:3 , 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

No data

Variant related genes	Relation type
ENSG00000231484	TF binding region
ENSG00000231232	TF binding region
ENSG00000271696	TF binding region
ENSG00000231484	CpG island
ENSG00000231232	CpG island
ENSG00000271696	CpG island

Extended variants
information (count: 11813 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:11813 , 50 per page) page: 1 2 3 4 5 6 7 ... 237

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566541042	chr7:57885902-57885903	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs28645626	chr7:57885906-57885907	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs533967450	chr7:57885908-57885909	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs2994340	chr7:57885913-57885914	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs111839664	chr7:57885918-57885919	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs558660332	chr7:57885926-57885927	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs577516638	chr7:57885940-57885941	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs12386594	chr7:57885941-57885942	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs373087304	chr7:57885948-57885949	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs544572041	chr7:57885949-57885950	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs556727620	chr7:57885955-57885956	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs575040420	chr7:57885959-57885960	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs199910711	chr7:57885960-57885961	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs111659973	chr7:57885966-57885967	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs200340121	chr7:57885981-57885982	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs79610510	chr7:57885984-57885985	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs73347409	chr7:57886011-57886012	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs527358928	chr7:57886026-57886027	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs199736617	chr7:57886033-57886034	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs200873574	chr7:57886034-57886035	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs113545308	chr7:57886036-57886037	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs545828779	chr7:57886043-57886044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs77722171	chr7:57886045-57886046	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs531643273	chr7:57886062-57886063	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs2994341	chr7:57886071-57886072	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs567933378	chr7:57886081-57886082	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs529018757	chr7:57886095-57886096	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs547171602	chr7:57886097-57886098	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs140964617	chr7:57886103-57886104	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs74416457	chr7:57886104-57886105	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs566654935	chr7:57886106-57886107	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs200724778	chr7:57886112-57886113	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs201882864	chr7:57886113-57886114	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs375692319	chr7:57886115-57886116	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs79537124	chr7:57886128-57886129	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs117736088	chr7:57886129-57886130	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs371630193	chr7:57886148-57886149	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs558953661	chr7:57886158-57886159	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs570718932	chr7:57886175-57886176	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs77850479	chr7:57886177-57886178	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs112425768	chr7:57886182-57886183	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs538535453	chr7:57886186-57886187	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs556551574	chr7:57886187-57886188	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs75132557	chr7:57886188-57886189	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs113931107	chr7:57886194-57886195	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs575102478	chr7:57886200-57886201	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs148606254	chr7:57886210-57886211	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs34505639	chr7:57886227-57886228	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs12386640	chr7:57886242-57886243	ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs12386641	chr7:57886243-57886244	ZNF genes & repeats	TF binding region	2 gene(s)	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:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:57885400-57886600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
2	chr7:57885400-57886600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:57885400-57886800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr7:57885800-57886800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
5	chr7:57886000-57886400	ZNF genes & repeats	Esophagus	oesophagus
6	chr7:57886000-57886400	ZNF genes & repeats	Pancreas	Pancrea
7	chr7:57886000-57886600	ZNF genes & repeats	Gastric	stomach
8	chr7:57886000-57886800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:57886200-57886800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:57917400-57918000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr7:57917800-57918400	Active TSS	Fetal Heart	heart
12	chr7:57918200-57918400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
13	chr7:57918200-57918800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr7:57925000-57925400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr7:57925400-57927000	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:57927000-57927200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr7:57927000-57927600	Active TSS	Liver	Liver
18	chr7:57927000-57927800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
19	chr7:57927000-57928200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:57927400-57927800	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
21	chr7:57927400-57929200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:57927600-57927800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
23	chr7:57927600-57927800	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr7:57927600-57927800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:57927600-57927800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:57927600-57927800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr7:57927600-57927800	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
28	chr7:57927600-57927800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
29	chr7:57927600-57927800	Flanking Bivalent TSS/Enh	Liver	Liver
30	chr7:57927600-57927800	Bivalent/Poised TSS	Brain Anterior Caudate	brain
31	chr7:57927600-57927800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
32	chr7:57927600-57927800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
33	chr7:57927600-57927800	Bivalent/Poised TSS	Left Ventricle	heart
34	chr7:57927600-57927800	Bivalent/Poised TSS	Right Atrium	heart
35	chr7:57927600-57927800	Bivalent/Poised TSS	Right Ventricle	heart
36	chr7:57927600-57927800	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
37	chr7:57927600-57928000	Bivalent/Poised TSS	Aorta	Aorta
38	chr7:57927600-57928000	Bivalent/Poised TSS	Monocytes-CD14+_RO01746	blood
39	chr7:57927600-57928200	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
40	chr7:57927600-57928200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:57927600-57928200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
42	chr7:57927600-57928200	Flanking Bivalent TSS/Enh	HMEC	breast
43	chr7:57927600-57928400	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
44	chr7:57927600-57928400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr7:57927600-57928400	Bivalent/Poised TSS	Brain Substantia Nigra	brain
46	chr7:57927600-57928400	Flanking Bivalent TSS/Enh	Placenta	Placenta
47	chr7:57927600-57928600	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
48	chr7:57927600-57928600	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
49	chr7:57927600-57928600	ZNF genes & repeats	Spleen	Spleen
50	chr7:57927600-57928800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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