Variant report

Variant	nsv877621
Chromosome Location	chr3:146117041-146172109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:210)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:210 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr3:146130261-146130561	K562	blood:	n/a	n/a
2	CBX3	chr3:146130211-146130634	K562	blood:	n/a	n/a
3	CBX3	chr3:146121518-146121906	HCT-116	colon:	n/a	n/a
4	CBX3	chr3:146163490-146163843	HCT-116	colon:	n/a	n/a
5	CEBPB	chr3:146140168-146140455	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr3:146120425-146120469	A549	lung:	n/a	n/a
7	CEBPB	chr3:146140161-146140507	MCF-7	breast:	n/a	n/a
8	CEBPB	chr3:146139507-146139992	MCF-7	breast:	n/a	n/a
9	CEBPB	chr3:146139531-146140133	A549	lung:	n/a	n/a
10	CHD2	chr3:146145207-146145271	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr3:146167520-146167670	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr3:146128660-146128810	HepG2	liver:	n/a	n/a
13	CTCF	chr3:146140280-146140430	MCF-7	breast:	n/a	n/a
14	CTCF	chr3:146140289-146140439	LNCaP	prostate:	n/a	n/a
15	CTCF	chr3:146128722-146128814	K562	blood:	n/a	n/a
16	CTCF	chr3:146140300-146140450	MCF-7	breast:	n/a	n/a
17	CTCF	chr3:146136520-146136670	MCF-7	breast:	n/a	n/a
18	CTCF	chr3:146158363-146158401	Fibrobl	skin:	n/a	n/a
19	CTCF	chr3:146140260-146140410	AoAF	blood vessel:	n/a	n/a
20	CTCF	chr3:146140300-146140450	HPF	lung:	n/a	n/a
21	CTCF	chr3:146140340-146140490	HMF	breast:	n/a	n/a
22	CTCF	chr3:146140340-146140490	HA-sp	spinal cord:	n/a	n/a
23	CTCF	chr3:146140905-146141193	IMR90	lung:	n/a	n/a
24	CTCF	chr3:146126503-146126564	K562	blood:	n/a	n/a
25	CTCF	chr3:146149340-146149490	MCF-7	breast:	n/a	n/a
26	CTCF	chr3:146140280-146140430	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr3:146140300-146140450	A549	lung:	n/a	n/a
28	CTCF	chr3:146150089-146150147	LNCaP	prostate:	n/a	n/a
29	CTCF	chr3:146140359-146140445	LNCaP	prostate:	n/a	n/a
30	CTCF	chr3:146140293-146140462	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr3:146140256-146140481	MCF-7	breast:	n/a	n/a
32	CTCF	chr3:146140300-146140450	NHEK	skin:	n/a	n/a
33	CTCF	chr3:146140240-146140390	HMF	breast:	n/a	n/a
34	CTCF	chr3:146140261-146140470	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:146130691-146130720	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr3:146167520-146167670	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:146128646-146128786	K562	blood:	n/a	n/a
38	CTCF	chr3:146121080-146121230	GM12874	blood:	n/a	n/a
39	CTCF	chr3:146140340-146140490	A549	lung:	n/a	n/a
40	CTCF	chr3:146140216-146140572	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:146140280-146140430	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr3:146140920-146141070	BJ	skin:	n/a	n/a
43	E2F4	chr3:146121715-146121899	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr3:146139619-146139919	MCF10A-Er-Src	breast:	n/a	n/a
45	ELF1	chr3:146139542-146140594	MCF-7	breast:	n/a	n/a
46	ELF1	chr3:146140143-146140516	A549	lung:	n/a	n/a
47	ELF1	chr3:146140062-146140558	MCF-7	breast:	n/a	n/a
48	ELK1	chr3:146143120-146143209	GM12878	blood:	n/a	n/a
49	ELK1	chr3:146140298-146140412	Hela-S3	cervix:	n/a	n/a
50	ELK4	chr3:146140126-146140481	Hela-S3	cervix:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:146129420-146129470	AG09309	skin:	n/a
2	chr3:146129360-146129410	BJ	skin:	n/a
3	chr3:146129264-146129314	HCF	heart:	n/a
4	chr3:146129264-146129314	PANC-1	pancreas:	n/a
5	chr3:146157056-146157106	H1-hESC	embryonic stem cell:	embryo
6	chr3:146129420-146129470	HEEpiC	esophagus:	n/a
7	chr3:146129420-146129470	BJ	skin:	n/a
8	chr3:146129420-146129470	HEK293	kidney:	embryo
9	chr3:146157056-146157106	AG09309	skin:	n/a
10	chr3:146129420-146129470	NB4	blood:	n/a
11	chr3:146129420-146129470	MCF10A-Er-Src	breast:	n/a
12	chr3:146129264-146129314	MCF-7	breast:	n/a
13	chr3:146129264-146129314	HIPEpiC	eye:	n/a
14	chr3:146129420-146129470	HAEpiC	amniotic membrane:	n/a
15	chr3:146157056-146157106	U87	brain:	n/a
16	chr3:146157056-146157106	SK-N-SH_RA	brain:	n/a
17	chr3:146129264-146129314	CMK	blood:	n/a
18	chr3:146129264-146129314	NHBE	bronchial:	n/a
19	chr3:146157056-146157106	HCPEpiC	choroid plexus:	n/a
20	chr3:146129360-146129410	GM19239	blood:	n/a
21	chr3:146157056-146157106	GM12892	blood:	n/a
22	chr3:146129264-146129314	HRPEpiC	eye:	n/a
23	chr3:146129360-146129410	GM12892	blood:	n/a
24	chr3:146129360-146129410	ovcar-3	ovarian:	n/a
25	chr3:146129264-146129314	ovcar-3	ovarian:	n/a
26	chr3:146129264-146129314	AG10803	skin:	n/a
27	chr3:146129264-146129314	HEK293	kidney:	embryo
28	chr3:146129264-146129314	Caco-2	colon:	n/a
29	chr3:146129420-146129470	RPTEC	kidney:	n/a
30	chr3:146129264-146129314	GM06990	blood:	n/a
31	chr3:146129360-146129410	GM12891	blood:	n/a
32	chr3:146129264-146129314	HCPEpiC	choroid plexus:	n/a
33	chr3:146157056-146157106	Caco-2	colon:	n/a
34	chr3:146129360-146129410	SAEC	small airway:	n/a
35	chr3:146129360-146129410	HEEpiC	esophagus:	n/a
36	chr3:146129264-146129314	NT2-D1	testis:	n/a
37	chr3:146129420-146129470	ECC-1	luminal epithelium:	n/a
38	chr3:146129264-146129314	ProgFib	skin:	n/a
39	chr3:146157056-146157106	Hela-S3	cervix:	n/a
40	chr3:146129264-146129314	SK-N-MC	brain:	n/a
41	chr3:146129420-146129470	AG09319	gingival:	n/a
42	chr3:146129420-146129470	T-47D	breast:	n/a
43	chr3:146129420-146129470	PrEC	prostate:	n/a
44	chr3:146129360-146129410	SK-N-SH	brain:	n/a
45	chr3:146157056-146157106	BJ	skin:	n/a
46	chr3:146129360-146129410	SK-N-SH_RA	brain:	n/a
47	chr3:146129420-146129470	BE2_C	brain:	n/a
48	chr3:146129360-146129410	HRPEpiC	eye:	n/a
49	chr3:146129360-146129410	NT2-D1	testis:	n/a
50	chr3:146129264-146129314	T-47D	breast:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:145879440..145881243-chr3:146138706..146140785,2	MCF-7	breast:
2	chr3:146139318..146141303-chr3:146183434..146185764,2	MCF-7	breast:
3	chr3:146139609..146141816-chr3:146146728..146148840,3	MCF-7	breast:
4	chr3:146139609..146141816-chr3:146146728..146148840,3	MCF-7	breast:
5	chr3:146137722..146139477-chr3:146142959..146145248,2	MCF-7	breast:
6	chr3:146142625..146144505-chr3:146147964..146150004,2	K562	blood:
7	chr3:146155934..146158732-chr3:146162320..146163882,2	MCF-7	breast:
8	chr3:146158561..146161277-chr3:146161473..146163225,2	K562	blood:
9	chr3:146139398..146141443-chr3:146220518..146223634,3	MCF-7	breast:
10	chr3:146137722..146139477-chr3:146142959..146145248,2	MCF-7	breast:
11	chr3:146168876..146171592-chr3:146171883..146173684,2	K562	blood:
12	chr3:146158889..146161569-chr3:146161974..146164517,2	MCF-7	breast:
13	chr3:146158889..146161569-chr3:146161974..146164517,2	MCF-7	breast:
14	chr3:146155934..146158732-chr3:146162320..146163882,2	MCF-7	breast:
15	chr3:146137952..146139503-chr3:146261134..146263708,2	MCF-7	breast:
16	chr3:146133340..146136821-chr3:146137357..146140210,3	MCF-7	breast:
17	chr3:146158561..146161277-chr3:146161473..146163225,2	K562	blood:
18	chr3:146142625..146144505-chr3:146147964..146150004,2	K562	blood:
19	chr3:146051931..146052494-chr3:146139879..146140654,2	MCF-7	breast:
20	chr3:146168876..146171592-chr3:146171883..146173684,2	K562	blood:
21	chr3:146169890..146171748-chr3:146177366..146178910,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLSCR2-1	chr3:146134291-146134390	NONHSAT092556
2	lnc-PLSCR2-1	chr3:146134293-146134364	NONHSAT092557
3	lnc-PLSCR2-1	chr3:146132912-146132954	NONHSAT092556
4	lnc-PLSCR2-1	chr3:146119147-146119346	NONHSAT092556
5	lnc-PLSCR2-1	chr3:146119142-146119363	NONHSAT092557

No data

Variant related genes	Relation type
ENSG00000241358	TF binding region
ENSG00000241358	CpG island
ENSG00000188313	chromatin interactions
ENSG00000163746	chromatin interactions
ENSG00000241358	chromatin interactions

Extended variants
information (count: 1775 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1775 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6803636	chr3:146117041-146117042	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561471137	chr3:146117044-146117045	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370946778	chr3:146117088-146117089	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76187681	chr3:146117142-146117143	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540840746	chr3:146117156-146117157	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12054308	chr3:146117168-146117169	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs532676401	chr3:146117185-146117186	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12053987	chr3:146117231-146117232	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs562987532	chr3:146117260-146117261	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112898850	chr3:146117282-146117283	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530071294	chr3:146117292-146117293	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548563331	chr3:146117324-146117325	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563186788	chr3:146117390-146117391	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192364781	chr3:146117392-146117393	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533787443	chr3:146117394-146117395	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145230399	chr3:146117474-146117475	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570275902	chr3:146117488-146117489	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149168165	chr3:146117523-146117524	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34851377	chr3:146117568-146117569	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79671785	chr3:146117570-146117571	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71158237	chr3:146117572-146117573	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28429479	chr3:146117577-146117578	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs28447268	chr3:146117583-146117584	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556011131	chr3:146117603-146117604	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574471397	chr3:146117624-146117625	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183604186	chr3:146117637-146117638	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115945553	chr3:146117660-146117661	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553876200	chr3:146117687-146117688	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186779760	chr3:146117695-146117696	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540902088	chr3:146117702-146117703	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565495621	chr3:146117704-146117705	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192658875	chr3:146117714-146117715	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544801866	chr3:146117765-146117766	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7650361	chr3:146117770-146117771	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs184848498	chr3:146117780-146117781	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539469475	chr3:146117788-146117789	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531397291	chr3:146117795-146117796	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140395178	chr3:146117830-146117831	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115375447	chr3:146117843-146117844	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7650546	chr3:146117850-146117851	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs143214920	chr3:146117923-146117924	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138806392	chr3:146117925-146117926	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552086137	chr3:146117931-146117932	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116399685	chr3:146117965-146117966	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140544852	chr3:146117971-146117972	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561684746	chr3:146117975-146117976	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34535967	chr3:146118031-146118032	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs541162745	chr3:146118056-146118057	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7628445	chr3:146118065-146118066	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs535486682	chr3:146118073-146118074	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146111800-146119400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:146118800-146119200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr3:146119200-146119400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr3:146119200-146121200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr3:146119400-146121000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:146119400-146122400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr3:146121000-146121200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr3:146121000-146121600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr3:146121000-146122400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:146121200-146121400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr3:146121200-146122200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr3:146121400-146121800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr3:146121600-146122000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr3:146121800-146122400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr3:146121800-146122600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr3:146122000-146122400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr3:146122000-146122800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr3:146122200-146122400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr3:146122200-146122600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr3:146122200-146122800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr3:146122200-146122800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr3:146122400-146122600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:146122400-146122800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr3:146122600-146122800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr3:146122600-146124800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:146122800-146123800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr3:146123400-146123600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr3:146123400-146124000	Enhancers	Fetal Lung	lung
29	chr3:146124000-146124200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr3:146124000-146125800	Weak transcription	Fetal Lung	lung
31	chr3:146124800-146125200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:146125200-146125600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr3:146125200-146125600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:146125600-146125800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:146125600-146127000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr3:146125800-146126200	Enhancers	Fetal Stomach	stomach
37	chr3:146125800-146126600	Enhancers	Fetal Lung	lung
38	chr3:146125800-146127800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:146127000-146127200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr3:146127800-146128400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:146128400-146129600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:146129600-146130000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:146129600-146130000	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr3:146130000-146130400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr3:146130000-146130400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
46	chr3:146130000-146132000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:146130400-146139400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr3:146130400-146142800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr3:146131400-146131800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr3:146134400-146135000	Enhancers	Colon Smooth Muscle	Colon

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