Variant report

Variant	nsv573002
Chromosome Location	chr16:76174188-76280843
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:355)
CpG islands
(count:610)
Chromatin interactive
region (count:8)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:355 , 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	ARID3A	chr16:76256042-76256283	HepG2	liver:	n/a	n/a
2	ATF2	chr16:76198817-76199366	GM12878	blood:	n/a	n/a
3	ATF2	chr16:76209888-76210374	GM12878	blood:	n/a	n/a
4	ATF2	chr16:76209899-76210415	GM12878	blood:	n/a	n/a
5	BACH1	chr16:76228619-76228977	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr16:76210041-76210280	GM12878	blood:	n/a	n/a
7	BHLHE40	chr16:76209948-76210288	GM12878	blood:	n/a	n/a
8	BHLHE40	chr16:76199039-76199164	GM12878	blood:	n/a	n/a
9	CEBPB	chr16:76256857-76257120	HepG2	liver:	n/a	chr16:76257002-76257013
10	CEBPB	chr16:76240016-76240289	HepG2	liver:	n/a	chr16:76240183-76240196 chr16:76240184-76240195
11	CEBPB	chr16:76266652-76266909	H1-hESC	embryonic stem cell:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
12	CEBPB	chr16:76266739-76266878	K562	blood:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
13	CEBPB	chr16:76276619-76276914	HepG2	liver:	n/a	chr16:76276751-76276762
14	CEBPB	chr16:76256803-76257198	H1-hESC	embryonic stem cell:	n/a	chr16:76257002-76257013
15	CEBPB	chr16:76220266-76220498	HepG2	liver:	n/a	chr16:76220342-76220353
16	CEBPB	chr16:76216964-76217158	HepG2	liver:	n/a	chr16:76217017-76217030 chr16:76217017-76217030
17	CEBPB	chr16:76266660-76266961	HepG2	liver:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
18	CEBPB	chr16:76266667-76266981	IMR90	lung:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
19	CEBPB	chr16:76190498-76190826	HepG2	liver:	n/a	n/a
20	CEBPB	chr16:76266695-76266926	A549	lung:	n/a	chr16:76266829-76266842 chr16:76266830-76266841 chr16:76266829-76266840 chr16:76266819-76266832 chr16:76266829-76266842
21	CEBPB	chr16:76190511-76190776	A549	lung:	n/a	n/a
22	CEBPB	chr16:76190493-76190837	IMR90	lung:	n/a	n/a
23	CEBPB	chr16:76200649-76200884	HepG2	liver:	n/a	n/a
24	CHD2	chr16:76210229-76210286	GM12878	blood:	n/a	n/a
25	CHD2	chr16:76191853-76191884	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr16:76191682-76191768	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr16:76191660-76191810	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr16:76261160-76261310	SAEC	small airway:	n/a	n/a
29	CTCF	chr16:76191620-76191770	GM12865	blood:	n/a	n/a
30	CTCF	chr16:76191627-76191863	GM12878	blood:	n/a	n/a
31	CTCF	chr16:76191620-76191770	GM12866	blood:	n/a	n/a
32	CTCF	chr16:76263161-76263202	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr16:76191600-76191750	Caco-2	colon:	n/a	n/a
34	CTCF	chr16:76191683-76191765	GM19238	blood:	n/a	n/a
35	CTCF	chr16:76191600-76191750	HepG2	liver:	n/a	n/a
36	CTCF	chr16:76191597-76191759	HepG2	liver:	n/a	n/a
37	CTCF	chr16:76191620-76191770	GM12871	blood:	n/a	n/a
38	CTCF	chr16:76232356-76232432	GM20000	blood:	n/a	n/a
39	CTCF	chr16:76191680-76191830	GM12875	blood:	n/a	n/a
40	CTCF	chr16:76191660-76191810	Caco-2	colon:	n/a	n/a
41	CTCF	chr16:76191517-76191837	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr16:76253820-76253970	GM12872	blood:	n/a	n/a
43	CTCF	chr16:76191660-76191810	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr16:76191684-76191687	K562	blood:	n/a	n/a
45	CTCF	chr16:76191600-76191750	GM12873	blood:	n/a	n/a
46	CTCF	chr16:76191671-76191758	MCF-7	breast:	n/a	n/a
47	CTCF	chr16:76191620-76191770	GM12873	blood:	n/a	n/a
48	CTCF	chr16:76191600-76191750	GM12869	blood:	n/a	n/a
49	CTCF	chr16:76245020-76245170	HPF	lung:	n/a	n/a
50	CTCF	chr16:76191640-76191790	SK-N-SH_RA	brain:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76269192-76269242	HepG2	liver:	n/a
2	chr16:76269192-76269242	Hela-S3	cervix:	n/a
3	chr16:76269184-76269234	NB4	blood:	n/a
4	chr16:76269297-76269347	A549	lung:	n/a
5	chr16:76228294-76228344	Caco-2	colon:	n/a
6	chr16:76269192-76269242	LNCaP	prostate:	n/a
7	chr16:76269297-76269347	MCF10A-Er-Src	breast:	n/a
8	chr16:76269192-76269242	CMK	blood:	n/a
9	chr16:76268785-76268835	A549	lung:	n/a
10	chr16:76269043-76269093	NHDF-neo	bronchial:	n/a
11	chr16:76269184-76269234	HL-60	blood:	n/a
12	chr16:76268785-76268835	HCF	heart:	n/a
13	chr16:76256948-76256998	PFSK-1	brain:	n/a
14	chr16:76256948-76256998	HCF	heart:	n/a
15	chr16:76269043-76269093	HepG2	liver:	n/a
16	chr16:76256948-76256998	ECC-1	luminal epithelium:	n/a
17	chr16:76272351-76272401	AG04450	lung:	fetal
18	chr16:76272351-76272401	HUVEC	blood vessel:	n/a
19	chr16:76272351-76272401	HRPEpiC	eye:	n/a
20	chr16:76272351-76272401	GM12892	blood:	n/a
21	chr16:76256948-76256998	PANC-1	pancreas:	n/a
22	chr16:76266534-76266584	BE2_C	brain:	n/a
23	chr16:76269409-76269459	Jurkat	blood:	n/a
24	chr16:76269409-76269459	HMEC	breast:	n/a
25	chr16:76268785-76268835	AG10803	skin:	n/a
26	chr16:76269297-76269347	HRPEpiC	eye:	n/a
27	chr16:76272351-76272401	SAEC	small airway:	n/a
28	chr16:76256948-76256998	AG09309	skin:	n/a
29	chr16:76269297-76269347	AG04449	skin:	fetal
30	chr16:76268785-76268835	AG04450	lung:	fetal
31	chr16:76268785-76268835	HRPEpiC	eye:	n/a
32	chr16:76256948-76256998	A549	lung:	n/a
33	chr16:76269297-76269347	HMEC	breast:	n/a
34	chr16:76269184-76269234	U87	brain:	n/a
35	chr16:76266534-76266584	K562	blood:	n/a
36	chr16:76269043-76269093	GM12891	blood:	n/a
37	chr16:76266534-76266584	MCF-7	breast:	n/a
38	chr16:76228294-76228344	GM12878	blood:	n/a
39	chr16:76269043-76269093	ovcar-3	ovarian:	n/a
40	chr16:76269409-76269459	AoSMC	blood vessel:	n/a
41	chr16:76269297-76269347	LNCaP	prostate:	n/a
42	chr16:76256948-76256998	HRPEpiC	eye:	n/a
43	chr16:76228294-76228344	BJ	skin:	n/a
44	chr16:76269184-76269234	NHBE	bronchial:	n/a
45	chr16:76269043-76269093	Hela-S3	cervix:	n/a
46	chr16:76266534-76266584	GM12878	blood:	n/a
47	chr16:76266534-76266584	HRPEpiC	eye:	n/a
48	chr16:76256948-76256998	NHBE	bronchial:	n/a
49	chr16:76256948-76256998	HEK293	kidney:	embryo
50	chr16:76266534-76266584	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:76167106..76169562-chr16:76172402..76175397,2	MCF-7	breast:
2	chr16:76272213..76274617-chr16:76275881..76278722,3	MCF-7	breast:
3	chr16:76170732..76173663-chr16:76174703..76177407,2	MCF-7	breast:
4	chr16:76267035..76268706-chr16:76269783..76271539,2	K562	blood:
5	chr16:76230231..76230851-chr2:70141294..70141952,2	Hela-S3	cervix:
6	chr16:76272213..76274617-chr16:76275881..76278722,3	MCF-7	breast:
7	chr16:76264260..76266317-chr16:76268267..76270250,2	MCF-7	breast:
8	chr16:76267035..76268706-chr16:76269783..76271539,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC025287.1-2	chr16:76174260-76174301	ENSG00000260223.1
2	lnc-AC025287.1-3	chr16:76268953-76269521	NONHSAT143777
3	lnc-AC025287.1-3	chr16:76262283-76262757	ENSG00000260983.1
4	lnc-AC025287.1-2	chr16:76181458-76181704	ENSG00000260223.1
5	lnc-AC025287.1-3	chr16:76268585-76269326	NONHSAT143776
6	lnc-AC025287.1-2	chr16:76181453-76181621	NONHSAT143772
7	lnc-AC025287.1-2	chr16:76181458-76181677	ENSG00000260223.1
8	lnc-AC025287.1-2	chr16:76181454-76181621	XLOC_012013
9	lnc-AC025287.1-3	chr16:76265215-76265343	ENSG00000260983.1

No data

Variant related genes	Relation type
ENSG00000260223	TF binding region
RPL18P13	TF binding region
ENSG00000260223	CpG island
RPL18P13	CpG island
ENSG00000244485	chromatin interactions

Extended variants
information (count: 3347 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3347 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1364132	chr16:76174188-76174189	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184973151	chr16:76174195-76174196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554213710	chr16:76174206-76174207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373330485	chr16:76174244-76174245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35403377	chr16:76174249-76174250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558847579	chr16:76174253-76174254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560076027	chr16:76174285-76174286	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs529017540	chr16:76174305-76174306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35502579	chr16:76174345-76174346	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs562543390	chr16:76174356-76174357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544049271	chr16:76174420-76174421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554234957	chr16:76174446-76174447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188633043	chr16:76174461-76174462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539795404	chr16:76174477-76174478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192823081	chr16:76174481-76174482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532805102	chr16:76174510-76174511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546162720	chr16:76174538-76174539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563222537	chr16:76174541-76174542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570240397	chr16:76174557-76174558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116070856	chr16:76174609-76174610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4888479	chr16:76174630-76174631	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs568523515	chr16:76174634-76174635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559987667	chr16:76174670-76174671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527811307	chr16:76174683-76174684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547779820	chr16:76174700-76174701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570743366	chr16:76174716-76174717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539849515	chr16:76174725-76174726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558571009	chr16:76174760-76174761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185302241	chr16:76174774-76174775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77719633	chr16:76174803-76174804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189222262	chr16:76174842-76174843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574166183	chr16:76174887-76174888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113657178	chr16:76174918-76174919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192560708	chr16:76174983-76174984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74025668	chr16:76174988-76174989	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs74025669	chr16:76175020-76175021	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs563002055	chr16:76175037-76175038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183574242	chr16:76175052-76175053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369615562	chr16:76175148-76175149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549324421	chr16:76175154-76175155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542415739	chr16:76175157-76175158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546718548	chr16:76175180-76175181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562285961	chr16:76175216-76175217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188263167	chr16:76175230-76175231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74025670	chr16:76175270-76175271	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs564649464	chr16:76175306-76175307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533165046	chr16:76175331-76175332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146932992	chr16:76175402-76175403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569009747	chr16:76175437-76175438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537769628	chr16:76175460-76175461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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

Chromatin state (count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76158200-76181400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr16:76174000-76176200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:76174200-76174600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr16:76174200-76175400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr16:76174400-76175800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr16:76175000-76175800	Enhancers	Brain Hippocampus Middle	brain
7	chr16:76175200-76175600	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr16:76175200-76175800	Enhancers	Brain Substantia Nigra	brain
9	chr16:76176600-76176800	Enhancers	Brain Angular Gyrus	brain
10	chr16:76179400-76179600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr16:76195200-76196200	Enhancers	Brain Substantia Nigra	brain
12	chr16:76196200-76196600	Weak transcription	Brain Substantia Nigra	brain
13	chr16:76196600-76197000	Enhancers	Brain Substantia Nigra	brain
14	chr16:76210000-76210400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr16:76210000-76210600	Active TSS	GM12878-XiMat	blood
16	chr16:76210400-76227600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr16:76215000-76216800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr16:76215600-76216400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr16:76215800-76216600	Enhancers	Adipose Nuclei	Adipose
20	chr16:76216000-76216200	Enhancers	Brain Cingulate Gyrus	brain
21	chr16:76216000-76216400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr16:76216000-76216600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr16:76216400-76216800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr16:76216800-76217200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr16:76226400-76229000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr16:76226600-76228400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr16:76226800-76229200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr16:76227000-76227200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr16:76227200-76227400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr16:76227200-76229000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr16:76227200-76229200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr16:76227200-76229400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr16:76227200-76229400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr16:76227400-76227600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr16:76227400-76227600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr16:76227400-76227600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr16:76227400-76228000	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr16:76227400-76228200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr16:76227400-76228400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr16:76227400-76229000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr16:76227400-76229000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr16:76227400-76229200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr16:76227400-76229200	Enhancers	HMEC	breast
44	chr16:76227400-76229400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr16:76227400-76229400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr16:76227600-76228000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr16:76227600-76228200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr16:76227600-76229000	Enhancers	Fetal Intestine Large	intestine
49	chr16:76227600-76229200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr16:76227600-76229200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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