Variant report

Variant	nsv591361
Chromosome Location	chr3:118901832-118909987
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:86)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:86 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr3:118903536-118904430	A549	lung:	n/a	n/a
2	ATF3	chr3:118903516-118904490	A549	lung:	n/a	n/a
3	BCL3	chr3:118903483-118904813	A549	lung:	n/a	n/a
4	BCL3	chr3:118903470-118904793	A549	lung:	n/a	n/a
5	CEBPB	chr3:118903501-118904647	A549	lung:	n/a	n/a
6	CEBPB	chr3:118903636-118904440	A549	lung:	n/a	n/a
7	CEBPB	chr3:118903666-118904068	IMR90	lung:	n/a	n/a
8	CEBPB	chr3:118903564-118904323	A549	lung:	n/a	n/a
9	CREB1	chr3:118903665-118903887	A549	lung:	n/a	n/a
10	CTCF	chr3:118908396-118908427	MCF-7	breast:	n/a	n/a
11	CTCF	chr3:118905659-118905693	Lung_OC	lung:	n/a	n/a
12	CTCF	chr3:118901860-118902010	GM12868	blood:	n/a	n/a
13	E2F6	chr3:118903934-118904952	A549	lung:	n/a	chr3:118904395-118904407 chr3:118904730-118904741
14	ELF1	chr3:118903677-118904070	A549	lung:	n/a	n/a
15	EP300	chr3:118903410-118904732	A549	lung:	n/a	n/a
16	EP300	chr3:118903420-118904691	A549	lung:	n/a	n/a
17	ETS1	chr3:118903540-118904291	A549	lung:	n/a	n/a
18	FOS	chr3:118903653-118904031	MCF10A-Er-Src	breast:	n/a	chr3:118903822-118903830
19	FOS	chr3:118903633-118904105	MCF10A-Er-Src	breast:	n/a	chr3:118903822-118903830
20	FOS	chr3:118905533-118905565	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr3:118903631-118904101	MCF10A-Er-Src	breast:	n/a	chr3:118903822-118903830
22	FOS	chr3:118903687-118903990	MCF10A-Er-Src	breast:	n/a	chr3:118903822-118903830
23	FOSL2	chr3:118903609-118904446	A549	lung:	n/a	chr3:118904406-118904417 chr3:118903822-118903830
24	FOSL2	chr3:118903472-118904587	A549	lung:	n/a	chr3:118904406-118904417 chr3:118903822-118903830
25	FOSL2	chr3:118903578-118904087	MCF-7	breast:	n/a	chr3:118903822-118903830
26	FOSL2	chr3:118903591-118904097	MCF-7	breast:	n/a	chr3:118903822-118903830
27	FOXA1	chr3:118903586-118903969	HepG2	liver:	n/a	chr3:118903737-118903749
28	FOXA1	chr3:118903606-118903923	HepG2	liver:	n/a	chr3:118903737-118903749
29	FOXA2	chr3:118903642-118903856	HepG2	liver:	n/a	chr3:118903737-118903749
30	FOXA2	chr3:118903508-118904465	A549	lung:	n/a	chr3:118903737-118903749
31	FOXA2	chr3:118903505-118904454	A549	lung:	n/a	chr3:118903737-118903749
32	GABPA	chr3:118903585-118904523	A549	lung:	n/a	n/a
33	GABPA	chr3:118903593-118904142	A549	lung:	n/a	n/a
34	GATA3	chr3:118902478-118902766	T-47D	breast:	n/a	chr3:118902705-118902715 chr3:118902708-118902715
35	GATA3	chr3:118903435-118904036	MCF-7	breast:	n/a	n/a
36	GATA3	chr3:118903533-118904826	A549	lung:	n/a	chr3:118904191-118904199 chr3:118904498-118904511
37	GATA3	chr3:118903598-118904575	A549	lung:	n/a	chr3:118904191-118904199 chr3:118904498-118904511
38	GATA3	chr3:118903503-118904079	MCF-7	breast:	n/a	n/a
39	JUND	chr3:118903519-118904477	A549	lung:	n/a	chr3:118904406-118904417 chr3:118903822-118903830
40	JUND	chr3:118903694-118904345	A549	lung:	n/a	chr3:118903822-118903830
41	MAX	chr3:118908702-118908781	NB4	blood:	n/a	chr3:118908730-118908740
42	MAX	chr3:118903564-118905008	A549	lung:	n/a	n/a
43	MAX	chr3:118900301-118901842	A549	lung:	n/a	n/a
44	MAX	chr3:118903555-118905093	A549	lung:	n/a	n/a
45	MAZ	chr3:118903575-118904130	IMR90	lung:	n/a	n/a
46	MYC	chr3:118903684-118903993	MCF10A-Er-Src	breast:	n/a	n/a
47	MYC	chr3:118903722-118903915	MCF10A-Er-Src	breast:	n/a	n/a
48	NR2F2	chr3:118903568-118903970	MCF-7	breast:	n/a	n/a
49	NR3C1	chr3:118903699-118903914	A549	lung:	n/a	n/a
50	NR3C1	chr3:118903653-118904265	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118906821-118906871	NT2-D1	testis:	n/a
2	chr3:118906821-118906871	HEEpiC	esophagus:	n/a
3	chr3:118906821-118906871	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:118903257-118903307	HNPCEpiC	eye:	n/a
5	chr3:118906821-118906871	HRCEpiC	kidney:	n/a
6	chr3:118903257-118903307	PFSK-1	brain:	n/a
7	chr3:118906821-118906871	SAEC	small airway:	n/a
8	chr3:118903257-118903307	GM12892	blood:	n/a
9	chr3:118906821-118906871	AG04450	lung:	fetal
10	chr3:118903257-118903307	A549	lung:	n/a
11	chr3:118903257-118903307	T-47D	breast:	n/a
12	chr3:118903257-118903307	SKMC	muscle:	n/a
13	chr3:118903257-118903307	Hela-S3	cervix:	n/a
14	chr3:118906821-118906871	HMEC	breast:	n/a
15	chr3:118906821-118906871	HCM	heart:	n/a
16	chr3:118903257-118903307	GM06990	blood:	n/a
17	chr3:118906821-118906871	AG04449	skin:	fetal
18	chr3:118906821-118906871	Hela-S3	cervix:	n/a
19	chr3:118903257-118903307	ProgFib	skin:	n/a
20	chr3:118903257-118903307	NB4	blood:	n/a
21	chr3:118906821-118906871	Hepatocyte	liver:	n/a
22	chr3:118906821-118906871	HepG2	liver:	n/a
23	chr3:118903257-118903307	HMEC	breast:	n/a
24	chr3:118903257-118903307	H1-hESC	embryonic stem cell:	embryo
25	chr3:118903257-118903307	HEEpiC	esophagus:	n/a
26	chr3:118903257-118903307	SAEC	small airway:	n/a
27	chr3:118903257-118903307	ovcar-3	ovarian:	n/a
28	chr3:118906821-118906871	PANC-1	pancreas:	n/a
29	chr3:118906821-118906871	GM12878	blood:	n/a
30	chr3:118903257-118903307	Jurkat	blood:	n/a
31	chr3:118903257-118903307	SK-N-MC	brain:	n/a
32	chr3:118906821-118906871	U87	brain:	n/a
33	chr3:118903257-118903307	MCF10A-Er-Src	breast:	n/a
34	chr3:118903257-118903307	AG04450	lung:	fetal
35	chr3:118903257-118903307	PANC-1	pancreas:	n/a
36	chr3:118903257-118903307	HRPEpiC	eye:	n/a
37	chr3:118906821-118906871	NHBE	bronchial:	n/a
38	chr3:118906821-118906871	SK-N-MC	brain:	n/a
39	chr3:118906821-118906871	HL-60	blood:	n/a
40	chr3:118903257-118903307	SK-N-SH	brain:	n/a
41	chr3:118903257-118903307	HAEpiC	amniotic membrane:	n/a
42	chr3:118903257-118903307	AG04449	skin:	fetal
43	chr3:118903257-118903307	Caco-2	colon:	n/a
44	chr3:118906821-118906871	Jurkat	blood:	n/a
45	chr3:118906821-118906871	Caco-2	colon:	n/a
46	chr3:118903257-118903307	HCPEpiC	choroid plexus:	n/a
47	chr3:118903257-118903307	CMK	blood:	n/a
48	chr3:118906821-118906871	SK-N-SH	brain:	n/a
49	chr3:118903257-118903307	SK-N-SH_RA	brain:	n/a
50	chr3:118903257-118903307	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:118904646..118906555-chr3:118909442..118912016,2	MCF-7	breast:
2	chr3:118894224..118896786-chr3:118901014..118905072,3	MCF-7	breast:
3	chr3:118903933..118906787-chr3:118956775..118959458,2	MCF-7	breast:
4	chr3:118900334..118903084-chr3:118903696..118906077,2	MCF-7	breast:
5	chr3:118903436..118905729-chr3:118907568..118909269,2	MCF-7	breast:
6	chr3:118898555..118900454-chr3:118903177..118905201,3	K562	blood:
7	chr3:118902403..118905431-chr3:118923096..118925754,3	MCF-7	breast:
8	chr3:118897325..118898996-chr3:118899726..118902200,2	MCF-7	breast:

No data

Variant related genes	Relation type
UPK1B	TF binding region
UPK1B	CpG island
ENSG00000114638	chromatin interactions
ENSG00000121578	chromatin interactions

Extended variants
information (count: 308 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6784773	chr3:118901832-118901833	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189701027	chr3:118901901-118901902	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs138474702	chr3:118901927-118901928	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs541396002	chr3:118901944-118901945	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs79103312	chr3:118902026-118902027	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs79993274	chr3:118902070-118902071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs115580555	chr3:118902082-118902083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs201941245	chr3:118902105-118902106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs11455368	chr3:118902108-118902109	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs374923734	chr3:118902109-118902110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545435865	chr3:118902115-118902116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs398062729	chr3:118902117-118902118	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73187809	chr3:118902118-118902119	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs114115313	chr3:118902119-118902120	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs528883990	chr3:118902121-118902122	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76788725	chr3:118902130-118902131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181135225	chr3:118902131-118902132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs79052701	chr3:118902132-118902133	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs62273511	chr3:118902134-118902135	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575915185	chr3:118902159-118902160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs566862504	chr3:118902180-118902181	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527835952	chr3:118902211-118902212	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs142993256	chr3:118902257-118902258	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs60465136	chr3:118902258-118902259	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537972978	chr3:118902265-118902266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs138886445	chr3:118902269-118902270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs149368846	chr3:118902275-118902276	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs562489768	chr3:118902290-118902291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144682201	chr3:118902297-118902298	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs367555114	chr3:118902298-118902299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554101058	chr3:118902329-118902330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs13071847	chr3:118902352-118902353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs539574457	chr3:118902366-118902367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs376686464	chr3:118902388-118902389	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576219578	chr3:118902405-118902406	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs186056552	chr3:118902423-118902424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs142790979	chr3:118902449-118902450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147441373	chr3:118902556-118902557	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs368761355	chr3:118902598-118902599	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs190470939	chr3:118902618-118902619	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs116007474	chr3:118902648-118902649	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs139735225	chr3:118902793-118902794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs4455314	chr3:118902844-118902845	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562449642	chr3:118902846-118902847	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs552707528	chr3:118902859-118902860	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564508702	chr3:118902865-118902866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531962332	chr3:118902910-118902911	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs145865181	chr3:118902947-118902948	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375086302	chr3:118902978-118902979	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs62273512	chr3:118902981-118902982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118884000-118914200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:118899000-118905000	Enhancers	Stomach Mucosa	stomach
3	chr3:118899600-118905200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:118899800-118904400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:118899800-118904800	Enhancers	Placenta Amnion	Placenta Amnion
6	chr3:118900000-118904800	Enhancers	HMEC	breast
7	chr3:118900600-118902200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr3:118900600-118904800	Enhancers	NHEK	skin
9	chr3:118900600-118908400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr3:118901000-118902800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr3:118901000-118903000	Weak transcription	NH-A	brain
12	chr3:118901000-118904000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:118901000-118904000	Weak transcription	NHDF-Ad	bronchial
14	chr3:118901000-118905400	Enhancers	Fetal Intestine Small	intestine
15	chr3:118901000-118924200	Weak transcription	Pancreas	Pancrea
16	chr3:118901200-118902800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:118901200-118902800	Weak transcription	Osteobl	bone
18	chr3:118901200-118903200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr3:118901400-118904000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr3:118901600-118902600	Weak transcription	Fetal Intestine Large	intestine
21	chr3:118901600-118902800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:118901600-118903800	Enhancers	A549	lung
23	chr3:118901800-118902200	Weak transcription	Placenta	Placenta
24	chr3:118902200-118902600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr3:118902200-118905000	Enhancers	Placenta	Placenta
26	chr3:118902600-118903400	Enhancers	Fetal Intestine Large	intestine
27	chr3:118902600-118904800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr3:118902800-118903400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr3:118902800-118903400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr3:118902800-118904600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr3:118902800-118904800	Enhancers	Osteobl	bone
32	chr3:118903000-118903200	Enhancers	NH-A	brain
33	chr3:118903200-118903400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr3:118903200-118903600	Weak transcription	NH-A	brain
35	chr3:118903400-118903800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr3:118903400-118903800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr3:118903400-118903800	Weak transcription	Fetal Intestine Large	intestine
38	chr3:118903400-118924200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr3:118903600-118903800	Enhancers	NH-A	brain
40	chr3:118903600-118904600	Enhancers	HepG2	liver
41	chr3:118903800-118904000	Flanking Active TSS	NH-A	brain
42	chr3:118903800-118904800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:118903800-118905000	Enhancers	Fetal Intestine Large	intestine
44	chr3:118903800-118905200	Flanking Active TSS	A549	lung
45	chr3:118903800-118908600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr3:118904000-118904200	Enhancers	NH-A	brain
47	chr3:118904000-118904400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr3:118904000-118904400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr3:118904000-118905400	Enhancers	NHDF-Ad	bronchial
50	chr3:118904200-118904400	Flanking Active TSS	NH-A	brain

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