Variant report

Variant	nsv1002567
Chromosome Location	chr3:112088498-112144063
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:499)
CpG islands
(count:367)
Chromatin interactive
region (count:3)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:499 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:112136351-112136756	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr3:112135258-112135975	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:112125881-112127134	GM12878	blood:	n/a	n/a
4	ATF2	chr3:112126396-112127097	GM12878	blood:	n/a	n/a
5	BACH1	chr3:112109999-112110295	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:112125920-112126324	GM12878	blood:	n/a	n/a
7	BATF	chr3:112126731-112127049	GM12878	blood:	n/a	n/a
8	BATF	chr3:112125953-112126291	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:112125982-112126312	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:112126457-112127059	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:112125955-112126331	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:112124731-112124980	GM12878	blood:	n/a	n/a
13	BCL3	chr3:112100567-112100977	GM12878	blood:	n/a	n/a
14	BCL3	chr3:112126018-112126314	GM12878	blood:	n/a	n/a
15	BCL3	chr3:112126377-112127030	GM12878	blood:	n/a	n/a
16	BCL3	chr3:112096538-112096914	GM12878	blood:	n/a	n/a
17	BCL3	chr3:112132440-112132881	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:112125784-112127013	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:112124814-112124883	GM12878	blood:	n/a	n/a
20	BRCA1	chr3:112097204-112097414	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:112126984-112127210	HepG2	liver:	n/a	chr3:112127108-112127119
22	CEBPB	chr3:112125534-112125626	HepG2	liver:	n/a	chr3:112125610-112125621
23	CEBPB	chr3:112093015-112093430	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:112113085-112113329	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:112127071-112127239	A549	lung:	n/a	chr3:112127108-112127119
26	CEBPB	chr3:112091185-112091519	HepG2	liver:	n/a	chr3:112091344-112091355
27	CEBPB	chr3:112091213-112091523	A549	lung:	n/a	chr3:112091344-112091355
28	CEBPB	chr3:112095684-112096873	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr3:112091255-112091521	IMR90	lung:	n/a	chr3:112091344-112091355
30	CEBPB	chr3:112125791-112127014	GM12878	blood:	n/a	n/a
31	CEBPB	chr3:112095783-112096092	A549	lung:	n/a	n/a
32	CEBPB	chr3:112109678-112110897	IMR90	lung:	n/a	chr3:112110019-112110027
33	CEBPB	chr3:112109597-112110853	Hela-S3	cervix:	n/a	chr3:112110019-112110027
34	CEBPB	chr3:112097320-112097540	IMR90	lung:	n/a	n/a
35	CEBPB	chr3:112091163-112091578	Hela-S3	cervix:	n/a	chr3:112091344-112091355
36	CEBPB	chr3:112127005-112127286	IMR90	lung:	n/a	chr3:112127108-112127119
37	CEBPB	chr3:112095724-112096413	IMR90	lung:	n/a	n/a
38	CEBPB	chr3:112095764-112096097	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:112097806-112098427	IMR90	lung:	n/a	n/a
40	CEBPB	chr3:112097151-112098213	Hela-S3	cervix:	n/a	n/a
41	CHD1	chr3:112126750-112126937	GM12878	blood:	n/a	n/a
42	CHD1	chr3:112136553-112136625	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr3:112119127-112119148	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr3:112119873-112119968	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr3:112137058-112137137	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr3:112140127-112140197	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr3:112095801-112096284	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr3:112110187-112110508	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr3:112109914-112110297	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr3:112135332-112136391	H1-hESC	embryonic stem cell:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:112117797-112117847	HNPCEpiC	eye:	n/a
2	chr3:112117797-112117847	HNPCEpiC	eye:	n/a
3	chr3:112096801-112096851	SK-N-MC	brain:	n/a
4	chr3:112135991-112136041	HCM	heart:	n/a
5	chr3:112117797-112117847	HCT-116	colon:	n/a
6	chr3:112143970-112144020	RPTEC	kidney:	n/a
7	chr3:112135991-112136041	U87	brain:	n/a
8	chr3:112096801-112096851	HIPEpiC	eye:	n/a
9	chr3:112113161-112113211	SAEC	small airway:	n/a
10	chr3:112113161-112113211	NT2-D1	testis:	n/a
11	chr3:112113161-112113211	MCF10A-Er-Src	breast:	n/a
12	chr3:112109797-112109847	CMK	blood:	n/a
13	chr3:112109797-112109847	AG09319	gingival:	n/a
14	chr3:112143970-112144020	AG04450	lung:	fetal
15	chr3:112096801-112096851	GM12878	blood:	n/a
16	chr3:112135991-112136041	A549	lung:	n/a
17	chr3:112113161-112113211	U87	brain:	n/a
18	chr3:112113161-112113211	HAEpiC	amniotic membrane:	n/a
19	chr3:112109797-112109847	SK-N-SH_RA	brain:	n/a
20	chr3:112109797-112109847	Hela-S3	cervix:	n/a
21	chr3:112096801-112096851	Caco-2	colon:	n/a
22	chr3:112143970-112144020	HIPEpiC	eye:	n/a
23	chr3:112113161-112113211	PrEC	prostate:	n/a
24	chr3:112096801-112096851	MCF-7	breast:	n/a
25	chr3:112096801-112096851	T-47D	breast:	n/a
26	chr3:112113161-112113211	H1-hESC	embryonic stem cell:	embryo
27	chr3:112113161-112113211	Jurkat	blood:	n/a
28	chr3:112143970-112144020	NHBE	bronchial:	n/a
29	chr3:112113161-112113211	BE2_C	brain:	n/a
30	chr3:112109797-112109847	HCM	heart:	n/a
31	chr3:112135991-112136041	PFSK-1	brain:	n/a
32	chr3:112096801-112096851	HCF	heart:	n/a
33	chr3:112096801-112096851	HRCEpiC	kidney:	n/a
34	chr3:112117797-112117847	GM12878	blood:	n/a
35	chr3:112096801-112096851	NB4	blood:	n/a
36	chr3:112143970-112144020	HNPCEpiC	eye:	n/a
37	chr3:112135991-112136041	BJ	skin:	n/a
38	chr3:112113161-112113211	GM12891	blood:	n/a
39	chr3:112109797-112109847	HPAEpiC	pulmonary alveolar:	n/a
40	chr3:112117797-112117847	AG04449	skin:	fetal
41	chr3:112109797-112109847	GM06990	blood:	n/a
42	chr3:112096801-112096851	ProgFib	skin:	n/a
43	chr3:112143970-112144020	Jurkat	blood:	n/a
44	chr3:112096801-112096851	NT2-D1	testis:	n/a
45	chr3:112117797-112117847	HRPEpiC	eye:	n/a
46	chr3:112109797-112109847	HEEpiC	esophagus:	n/a
47	chr3:112117797-112117847	AG04450	lung:	fetal
48	chr3:112135991-112136041	GM19239	blood:	n/a
49	chr3:112113161-112113211	SK-N-SH	brain:	n/a
50	chr3:112109797-112109847	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:111832694..111835578-chr3:112096846..112099201,2	MCF-7	breast:
2	chr3:112090607..112092226-chr3:112097134..112099677,2	MCF-7	breast:
3	chr3:112090607..112092226-chr3:112097134..112099677,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTLA-1	chr3:112127921-112127994	NONHSAT091172
2	lnc-BTLA-1	chr3:112099217-112099448	NONHSAT091176
3	lnc-BTLA-1	chr3:112099250-112099670	NONHSAT091173
4	lnc-BTLA-1	chr3:112127921-112127981	ENSG00000243081
5	lnc-BTLA-1	chr3:112127921-112128049	NONHSAT091169
6	lnc-BTLA-1	chr3:112099250-112099448	NONHSAT091172
7	lnc-BTLA-1	chr3:112115494-112116995	ENSG00000243081
8	lnc-BTLA-1	chr3:112099250-112099448	NONHSAT091168
9	lnc-BTLA-1	chr3:112100753-112100776	NONHSAT091168
10	lnc-BTLA-1	chr3:112100753-112100780	NONHSAT091174
11	lnc-BTLA-1	chr3:112123200-112123225	NONHSAT091170
12	lnc-BTLA-1	chr3:112100753-112100776	NONHSAT091176
13	lnc-BTLA-4	chr3:112130091-112130571	NONHSAT091178
14	lnc-BTLA-1	chr3:112127921-112127951	NONHSAT091167
15	lnc-BTLA-1	chr3:112099250-112099448	NONHSAT091174

No data

Variant related genes	Relation type
ENSG00000243081	TF binding region
ENSG00000243081	CpG island

Extended variants
information (count: 2051 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2051 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7648553	chr3:112088498-112088499	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183037888	chr3:112088519-112088520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560542063	chr3:112088522-112088523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545291457	chr3:112088552-112088553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565276152	chr3:112088564-112088565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115722229	chr3:112088586-112088587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377532631	chr3:112088703-112088704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561343764	chr3:112088747-112088748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186241636	chr3:112088801-112088802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71134827	chr3:112088868-112088869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199969511	chr3:112088869-112088870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140270324	chr3:112088929-112088930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs71134828	chr3:112088937-112088938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2399424	chr3:112088939-112088940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559834346	chr3:112089090-112089091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550307433	chr3:112089117-112089118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563670174	chr3:112089128-112089129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532592545	chr3:112089152-112089153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552485830	chr3:112089202-112089203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190664340	chr3:112089225-112089226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548674803	chr3:112089238-112089239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4339085	chr3:112089255-112089256	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs537100668	chr3:112089259-112089260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537204051	chr3:112089289-112089290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556682390	chr3:112089293-112089294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182498656	chr3:112089309-112089310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539078546	chr3:112089348-112089349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2399425	chr3:112089351-112089352	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs568891475	chr3:112089352-112089353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570633939	chr3:112089385-112089386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527518976	chr3:112089406-112089407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531382452	chr3:112089424-112089425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572670556	chr3:112089459-112089460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541376634	chr3:112089467-112089468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187247147	chr3:112089481-112089482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371526953	chr3:112089490-112089491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574980363	chr3:112089507-112089508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543926075	chr3:112089550-112089551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563807813	chr3:112089590-112089591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115929249	chr3:112089602-112089603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192189702	chr3:112089618-112089619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139333638	chr3:112089633-112089634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150047947	chr3:112089761-112089762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548193728	chr3:112089762-112089763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571620526	chr3:112089837-112089838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145402450	chr3:112089859-112089860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7621578	chr3:112089865-112089866	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs182984754	chr3:112089897-112089898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534057117	chr3:112089959-112089960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115326970	chr3:112089983-112089984	Weak transcription	n/a	n/a	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
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	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
Neurodevelopmental disorder	22521361	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
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Breast cancer	22522925	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1047 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112066000-112089800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:112069200-112095400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr3:112070600-112088800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:112070800-112090600	Weak transcription	Brain Hippocampus Middle	brain
5	chr3:112077200-112094200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr3:112077600-112107200	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr3:112080000-112088800	Weak transcription	Colon Smooth Muscle	Colon
8	chr3:112080000-112096000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr3:112081000-112088800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr3:112081200-112092800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr3:112081400-112091600	Weak transcription	Primary T cells from cord blood	blood
12	chr3:112082200-112096000	Weak transcription	Fetal Stomach	stomach
13	chr3:112082600-112094600	Weak transcription	Brain Anterior Caudate	brain
14	chr3:112083400-112092200	Weak transcription	Primary B cells from cord blood	blood
15	chr3:112083800-112090600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr3:112083800-112092200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr3:112084000-112090600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr3:112084000-112094800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr3:112084200-112092600	Weak transcription	Fetal Kidney	kidney
20	chr3:112084400-112091600	Weak transcription	Placenta	Placenta
21	chr3:112084600-112093200	Weak transcription	Fetal Lung	lung
22	chr3:112084800-112088800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr3:112084800-112096000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr3:112084800-112096800	Weak transcription	Fetal Muscle Leg	muscle
25	chr3:112085000-112089800	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr3:112085000-112095600	Weak transcription	Thymus	Thymus
27	chr3:112085400-112096000	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr3:112085600-112095400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr3:112085600-112096000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:112085800-112089200	Weak transcription	Fetal Brain Female	brain
31	chr3:112085800-112091400	Weak transcription	Primary B cells from peripheral blood	blood
32	chr3:112085800-112091400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr3:112085800-112091400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr3:112085800-112092200	Weak transcription	Primary hematopoietic stem cells	blood
35	chr3:112085800-112096400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr3:112085800-112096600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr3:112085800-112101400	Weak transcription	Aorta	Aorta
38	chr3:112086000-112095000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr3:112086000-112095600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:112086200-112091200	Weak transcription	Brain Angular Gyrus	brain
41	chr3:112086200-112091400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr3:112086200-112092200	Weak transcription	Fetal Thymus	thymus
43	chr3:112087600-112096400	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr3:112088000-112089600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr3:112088000-112090600	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr3:112088200-112089800	Weak transcription	Brain Germinal Matrix	brain
47	chr3:112088200-112092800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr3:112088400-112091400	Weak transcription	Adipose Nuclei	Adipose
49	chr3:112089600-112090200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr3:112090200-112090400	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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