Variant report

Variant	nsv573019
Chromosome Location	chr16:76272617-76318640
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:380)
CpG islands
(count:245)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr16:76312973-76313007	K562	blood:	n/a	chr16:76312985-76312998 chr16:76312985-76312998 chr16:76312985-76312996
2	CEBPB	chr16:76276619-76276914	HepG2	liver:	n/a	chr16:76276751-76276762
3	CEBPB	chr16:76312850-76313163	IMR90	lung:	n/a	chr16:76312985-76312998 chr16:76312985-76312998 chr16:76312985-76312996
4	CEBPB	chr16:76312863-76313217	H1-hESC	embryonic stem cell:	n/a	chr16:76312985-76312998 chr16:76312985-76312998 chr16:76312985-76312996
5	CEBPB	chr16:76312811-76313131	HepG2	liver:	n/a	chr16:76312985-76312998 chr16:76312985-76312998 chr16:76312985-76312996
6	CEBPB	chr16:76312785-76313180	MCF-7	breast:	n/a	chr16:76312985-76312998 chr16:76312985-76312998 chr16:76312985-76312996
7	CEBPB	chr16:76297599-76297930	HepG2	liver:	n/a	chr16:76297751-76297762
8	CEBPB	chr16:76302668-76302719	HepG2	liver:	n/a	chr16:76302697-76302708
9	CEBPB	chr16:76312838-76313126	A549	lung:	n/a	chr16:76312985-76312998 chr16:76312985-76312998 chr16:76312985-76312996
10	CEBPB	chr16:76297646-76297827	H1-hESC	embryonic stem cell:	n/a	chr16:76297751-76297762
11	CHD2	chr16:76311092-76311304	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr16:76299414-76299678	Gliobla	brain:	n/a	n/a
13	CTCF	chr16:76299460-76299610	GM12870	blood:	n/a	n/a
14	CTCF	chr16:76299435-76299603	K562	blood:	n/a	n/a
15	CTCF	chr16:76299460-76299610	GM12878	blood:	n/a	n/a
16	CTCF	chr16:76299460-76299610	GM12871	blood:	n/a	n/a
17	CTCF	chr16:76299450-76299669	HepG2	liver:	n/a	n/a
18	CTCF	chr16:76299440-76299590	GM12868	blood:	n/a	n/a
19	CTCF	chr16:76312948-76313209	H1-hESC	embryonic stem cell:	n/a	chr16:76313098-76313119
20	CTCF	chr16:76299480-76299630	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr16:76299480-76299630	HCT-116	colon:	n/a	n/a
22	CTCF	chr16:76313060-76313210	NHEK	skin:	n/a	chr16:76313098-76313119
23	CTCF	chr16:76299520-76299670	AG10803	skin:	n/a	n/a
24	CTCF	chr16:76299460-76299610	HepG2	liver:	n/a	n/a
25	CTCF	chr16:76299460-76299610	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr16:76299500-76299650	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr16:76299500-76299650	GM12864	blood:	n/a	n/a
28	CTCF	chr16:76299460-76299610	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr16:76299459-76299603	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr16:76313040-76313190	HMF	breast:	n/a	chr16:76313098-76313119
31	CTCF	chr16:76312700-76312850	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr16:76313120-76313270	BE2_C	brain:	n/a	n/a
33	CTCF	chr16:76299427-76299634	LNCaP	prostate:	n/a	n/a
34	CTCF	chr16:76299460-76299610	GM12868	blood:	n/a	n/a
35	CTCF	chr16:76299460-76299610	AG04450	lung:	n/a	n/a
36	CTCF	chr16:76299440-76299590	HEK293	kidney:	n/a	n/a
37	CTCF	chr16:76313020-76313170	AoAF	blood vessel:	n/a	chr16:76313098-76313119
38	CTCF	chr16:76299460-76299610	GM12801	blood:	n/a	n/a
39	CTCF	chr16:76313060-76313210	HPF	lung:	n/a	chr16:76313098-76313119
40	CTCF	chr16:76313040-76313190	HPAF	blood vessel:	n/a	chr16:76313098-76313119
41	CTCF	chr16:76299440-76299590	HCM	heart:	n/a	n/a
42	CTCF	chr16:76313020-76313170	HCFaa	heart:	n/a	chr16:76313098-76313119
43	CTCF	chr16:76299428-76299668	GM12878	blood:	n/a	n/a
44	CTCF	chr16:76313000-76313150	GM12872	blood:	n/a	chr16:76313098-76313119
45	CTCF	chr16:76299335-76299742	GM12878	blood:	n/a	n/a
46	CTCF	chr16:76312680-76312830	BE2_C	brain:	n/a	n/a
47	CTCF	chr16:76299480-76299630	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr16:76313002-76313239	K562	blood:	n/a	chr16:76313098-76313119
49	CTCF	chr16:76299430-76299660	MCF-7	breast:	n/a	n/a
50	CTCF	chr16:76313020-76313170	HPAF	blood vessel:	n/a	chr16:76313098-76313119

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76309968-76310018	T-47D	breast:	n/a
2	chr16:76309968-76310018	T-47D	breast:	n/a
3	chr16:76309968-76310018	CMK	blood:	n/a
4	chr16:76311266-76311316	SK-N-MC	brain:	n/a
5	chr16:76309968-76310018	HMEC	breast:	n/a
6	chr16:76309968-76310018	HRE	kidney:	n/a
7	chr16:76311050-76311100	AG09309	skin:	n/a
8	chr16:76309968-76310018	HAEpiC	amniotic membrane:	n/a
9	chr16:76311266-76311316	AG04449	skin:	fetal
10	chr16:76310816-76310866	MCF-7	breast:	n/a
11	chr16:76311266-76311316	NH-A	brain:	n/a
12	chr16:76310816-76310866	SK-N-MC	brain:	n/a
13	chr16:76311050-76311100	ECC-1	luminal epithelium:	n/a
14	chr16:76310816-76310866	PFSK-1	brain:	n/a
15	chr16:76309968-76310018	HIPEpiC	eye:	n/a
16	chr16:76311266-76311316	HEK293	kidney:	embryo
17	chr16:76311266-76311316	T-47D	breast:	n/a
18	chr16:76311266-76311316	Hela-S3	cervix:	n/a
19	chr16:76311050-76311100	MCF10A-Er-Src	breast:	n/a
20	chr16:76309968-76310018	K562	blood:	n/a
21	chr16:76309968-76310018	LNCaP	prostate:	n/a
22	chr16:76309968-76310018	HRCEpiC	kidney:	n/a
23	chr16:76309968-76310018	HRPEpiC	eye:	n/a
24	chr16:76311266-76311316	PFSK-1	brain:	n/a
25	chr16:76311050-76311100	SAEC	small airway:	n/a
26	chr16:76309968-76310018	MCF-7	breast:	n/a
27	chr16:76309968-76310018	HPAEpiC	pulmonary alveolar:	n/a
28	chr16:76311050-76311100	ovcar-3	ovarian:	n/a
29	chr16:76311050-76311100	HAEpiC	amniotic membrane:	n/a
30	chr16:76309968-76310018	SAEC	small airway:	n/a
31	chr16:76310816-76310866	T-47D	breast:	n/a
32	chr16:76310816-76310866	Jurkat	blood:	n/a
33	chr16:76309968-76310018	ovcar-3	ovarian:	n/a
34	chr16:76311050-76311100	NB4	blood:	n/a
35	chr16:76309968-76310018	PFSK-1	brain:	n/a
36	chr16:76309968-76310018	AG04450	lung:	fetal
37	chr16:76311266-76311316	GM12892	blood:	n/a
38	chr16:76311266-76311316	AG04450	lung:	fetal
39	chr16:76310816-76310866	ProgFib	skin:	n/a
40	chr16:76310816-76310866	NHDF-neo	bronchial:	n/a
41	chr16:76311266-76311316	HCF	heart:	n/a
42	chr16:76309968-76310018	AG09309	skin:	n/a
43	chr16:76311266-76311316	Jurkat	blood:	n/a
44	chr16:76309968-76310018	IMR90	lung:	fetal
45	chr16:76311266-76311316	PANC-1	pancreas:	n/a
46	chr16:76311050-76311100	AG10803	skin:	n/a
47	chr16:76309968-76310018	AG09319	gingival:	n/a
48	chr16:76311266-76311316	RPTEC	kidney:	n/a
49	chr16:76310816-76310866	AG09319	gingival:	n/a
50	chr16:76311266-76311316	GM12878	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:76312786..76313346-chr16:77205382..77206025,2	MCF-7	breast:
2	chr16:76294288..76297210-chr16:76297398..76300230,2	K562	blood:
3	chr16:76272213..76274617-chr16:76275881..76278722,3	MCF-7	breast:
4	chr16:76307042..76309067-chr16:76309191..76311472,2	K562	blood:
5	chr16:76313028..76313530-chr16:77203611..77204279,2	MCF-7	breast:
6	chr16:76312365..76313607-chr16:76673596..76674287,4	MCF-7	breast:
7	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
8	chr16:76272213..76274617-chr16:76275881..76278722,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC025287.1-3	chr16:76296129-76296263	ENSG00000260983.1
2	lnc-AC025287.1-3	chr16:76296129-76296234	NONHSAT143776

No data

Variant related genes	Relation type
ENSG00000260983	TF binding region
RPL18P13	TF binding region
CNTNAP4	TF binding region
RN7SKP233	TF binding region
ENSG00000260983	CpG island
RPL18P13	CpG island
CNTNAP4	CpG island
RN7SKP233	CpG island
ENSG00000152910	chromatin interactions
ENSG00000260983	chromatin interactions

Extended variants
information (count: 841 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558523892	chr16:76273697-76273698	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs72794930	chr16:76273713-76273714	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs555418566	chr16:76274601-76274602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149247841	chr16:76274620-76274621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562303613	chr16:76274634-76274635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541755725	chr16:76274636-76274637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560971250	chr16:76274649-76274650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144582788	chr16:76274673-76274674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543487487	chr16:76274674-76274675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563411632	chr16:76274681-76274682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531505911	chr16:76274735-76274736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371081254	chr16:76274750-76274751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188599527	chr16:76274757-76274758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548921946	chr16:76274768-76274769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566070665	chr16:76274771-76274772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371652396	chr16:76274787-76274788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547340289	chr16:76275409-76275410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535535516	chr16:76275419-76275420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116344056	chr16:76275439-76275440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12596723	chr16:76275447-76275448	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
21	rs146011048	chr16:76275448-76275449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536336348	chr16:76275466-76275467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78579137	chr16:76275481-76275482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549994905	chr16:76275493-76275494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187048086	chr16:76275533-76275534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537349959	chr16:76275540-76275541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375025386	chr16:76275569-76275570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60507614	chr16:76275613-76275614	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573939293	chr16:76275628-76275629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377060407	chr16:76275646-76275647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542698782	chr16:76275660-76275661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559827369	chr16:76275690-76275691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190385363	chr16:76275695-76275696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528845399	chr16:76275724-76275725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140073569	chr16:76275772-76275773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs72794931	chr16:76275778-76275779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182959430	chr16:76275783-76275784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533216448	chr16:76275785-76275786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111883418	chr16:76275794-76275795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556802141	chr16:76275797-76275798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs386792249	chr16:76290605-76290606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs151004372	chr16:76290607-76290608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140902300	chr16:76290623-76290624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145934253	chr16:76290629-76290630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs193075621	chr16:76290646-76290647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556782519	chr16:76290666-76290667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563559470	chr16:76290705-76290706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369781914	chr16:76290718-76290719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147836906	chr16:76290719-76290720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374547491	chr16:76290727-76290728	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	24585490	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76274600-76274800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr16:76275400-76275800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr16:76290600-76291400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr16:76291400-76291600	Enhancers	Gastric	stomach
5	chr16:76299200-76299800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr16:76302600-76302800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr16:76302800-76303400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr16:76303400-76304000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr16:76306600-76307200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr16:76307000-76309200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr16:76307200-76310800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr16:76307800-76309200	Enhancers	Osteobl	bone
13	chr16:76308200-76308400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr16:76308800-76309000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr16:76309800-76310400	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr16:76310000-76310200	Enhancers	Brain Substantia Nigra	brain
17	chr16:76310000-76310600	Enhancers	Brain Angular Gyrus	brain
18	chr16:76310200-76310400	Enhancers	Fetal Brain Male	brain
19	chr16:76310200-76310600	Enhancers	Brain Cingulate Gyrus	brain
20	chr16:76310200-76310600	Enhancers	Fetal Brain Female	brain
21	chr16:76310200-76310800	Enhancers	Brain Germinal Matrix	brain
22	chr16:76310200-76310800	Enhancers	Brain Hippocampus Middle	brain
23	chr16:76310400-76310800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr16:76310400-76310800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr16:76310400-76310800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
26	chr16:76310400-76310800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr16:76310400-76310800	Flanking Active TSS	Fetal Brain Male	brain
28	chr16:76310400-76315200	Active TSS	Brain Anterior Caudate	brain
29	chr16:76310600-76311000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
30	chr16:76310600-76311000	Flanking Active TSS	Fetal Brain Female	brain
31	chr16:76310600-76313400	Active TSS	Brain Angular Gyrus	brain
32	chr16:76310800-76311000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr16:76310800-76311000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
34	chr16:76310800-76311200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
35	chr16:76310800-76311200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr16:76310800-76311200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr16:76310800-76311200	Flanking Active TSS	Brain Germinal Matrix	brain
38	chr16:76310800-76311200	Enhancers	Colon Smooth Muscle	Colon
39	chr16:76310800-76311200	Bivalent Enhancer	Fetal Lung	lung
40	chr16:76310800-76311400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr16:76310800-76311600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
42	chr16:76310800-76311600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr16:76310800-76311600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr16:76310800-76311600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
45	chr16:76310800-76311600	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
46	chr16:76310800-76312200	Active TSS	Fetal Brain Male	brain
47	chr16:76310800-76313000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr16:76310800-76313400	Active TSS	Brain Substantia Nigra	brain
49	chr16:76310800-76315400	Active TSS	Brain Cingulate Gyrus	brain
50	chr16:76310800-76315400	Active TSS	Brain Hippocampus Middle	brain

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