Variant report

Variant	nsv592079
Chromosome Location	chr3:155474879-155493915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:155487617-155487877	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr3:155487792-155488163	K562	blood:	n/a	n/a
3	CEBPB	chr3:155484017-155484279	K562	blood:	n/a	n/a
4	CEBPB	chr3:155487735-155487999	K562	blood:	n/a	n/a
5	CEBPB	chr3:155481714-155482101	A549	lung:	n/a	n/a
6	CEBPB	chr3:155477996-155478082	IMR90	lung:	n/a	n/a
7	CEBPB	chr3:155483934-155484389	MCF-7	breast:	n/a	chr3:155484369-155484386
8	CEBPB	chr3:155481678-155482001	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:155484002-155484366	A549	lung:	n/a	n/a
10	CEBPB	chr3:155487739-155488080	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr3:155484031-155484340	K562	blood:	n/a	n/a
12	CEBPB	chr3:155484008-155484489	Hela-S3	cervix:	n/a	chr3:155484369-155484386
13	CEBPB	chr3:155477835-155478185	K562	blood:	n/a	n/a
14	CEBPB	chr3:155481686-155482016	IMR90	lung:	n/a	n/a
15	CEBPB	chr3:155481693-155482017	A549	lung:	n/a	n/a
16	CEBPB	chr3:155483987-155484490	IMR90	lung:	n/a	chr3:155484369-155484386
17	CEBPB	chr3:155481705-155482029	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:155477873-155478193	K562	blood:	n/a	n/a
19	CEBPB	chr3:155476076-155476236	K562	blood:	n/a	chr3:155476115-155476128
20	CEBPB	chr3:155477961-155478093	A549	lung:	n/a	n/a
21	CEBPB	chr3:155481680-155482057	K562	blood:	n/a	n/a
22	CTCF	chr3:155487720-155487870	GM12875	blood:	n/a	n/a
23	FOS	chr3:155484040-155484309	HUVEC	blood vessel:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198 chr3:155484188-155484199
24	FOS	chr3:155483956-155484408	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198 chr3:155484188-155484199
25	FOS	chr3:155483951-155484366	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198 chr3:155484188-155484199
26	FOS	chr3:155483934-155484477	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198 chr3:155484188-155484199
27	FOS	chr3:155483930-155484451	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198 chr3:155484188-155484199
28	FOSL2	chr3:155484008-155484407	MCF-7	breast:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
29	FOSL2	chr3:155483979-155484315	A549	lung:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
30	FOSL2	chr3:155484053-155484254	A549	lung:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
31	JUN	chr3:155484040-155484388	HepG2	liver:	n/a	chr3:155484190-155484197 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
32	JUND	chr3:155484017-155484384	Hela-S3	cervix:	n/a	chr3:155484190-155484197 chr3:155484188-155484199 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
33	JUND	chr3:155484016-155484379	HepG2	liver:	n/a	chr3:155484190-155484197 chr3:155484188-155484199 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
34	JUND	chr3:155483864-155484516	SK-N-SH	brain:	n/a	chr3:155484190-155484197 chr3:155484188-155484199 chr3:155484188-155484200 chr3:155484190-155484199 chr3:155484189-155484199 chr3:155484190-155484198 chr3:155484189-155484198
35	KAP1	chr3:155487787-155488193	HEK293	kidney:	n/a	n/a
36	KAP1	chr3:155487841-155488191	K562	blood:	n/a	n/a
37	MAFK	chr3:155487661-155487892	H1-hESC	embryonic stem cell:	n/a	n/a
38	MAX	chr3:155484039-155484148	A549	lung:	n/a	n/a
39	MXI1	chr3:155492134-155492147	H1-hESC	embryonic stem cell:	n/a	n/a
40	MYC	chr3:155484018-155484263	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484199 chr3:155484189-155484198
41	MYC	chr3:155488776-155488807	MCF-7	breast:	n/a	n/a
42	MYC	chr3:155483937-155484362	MCF10A-Er-Src	breast:	n/a	chr3:155484190-155484199 chr3:155484189-155484198
43	NFYB	chr3:155484018-155484218	GM12878	blood:	n/a	chr3:155484146-155484156
44	POLR2A	chr3:155474993-155476040	K562	blood:	n/a	n/a
45	POLR2A	chr3:155489293-155489294	K562	blood:	n/a	n/a
46	POLR2A	chr3:155480024-155480225	K562	blood:	n/a	n/a
47	POLR2A	chr3:155488073-155488110	MCF-7	breast:	n/a	n/a
48	POLR2A	chr3:155482408-155482886	K562	blood:	n/a	n/a
49	POLR2A	chr3:155492402-155492404	MCF-7	breast:	n/a	n/a
50	POLR2A	chr3:155488165-155488194	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:155480645-155480695	GM19239	blood:	n/a
2	chr3:155480645-155480695	Hepatocyte	liver:	n/a
3	chr3:155480645-155480695	HRPEpiC	eye:	n/a
4	chr3:155480645-155480695	SKMC	muscle:	n/a
5	chr3:155480645-155480695	GM12891	blood:	n/a
6	chr3:155480645-155480695	U87	brain:	n/a
7	chr3:155480645-155480695	SK-N-MC	brain:	n/a
8	chr3:155480645-155480695	A549	lung:	n/a
9	chr3:155480645-155480695	PrEC	prostate:	n/a
10	chr3:155480645-155480695	GM12878	blood:	n/a
11	chr3:155480645-155480695	K562	blood:	n/a
12	chr3:155480645-155480695	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:155480645-155480695	LNCaP	prostate:	n/a
14	chr3:155480645-155480695	Hela-S3	cervix:	n/a
15	chr3:155480645-155480695	BE2_C	brain:	n/a
16	chr3:155480645-155480695	T-47D	breast:	n/a
17	chr3:155480645-155480695	HRCEpiC	kidney:	n/a
18	chr3:155480645-155480695	ProgFib	skin:	n/a
19	chr3:155480645-155480695	PANC-1	pancreas:	n/a
20	chr3:155480645-155480695	AG04449	skin:	fetal
21	chr3:155480645-155480695	HRE	kidney:	n/a
22	chr3:155480645-155480695	HCM	heart:	n/a
23	chr3:155480645-155480695	ECC-1	luminal epithelium:	n/a
24	chr3:155480645-155480695	MCF-7	breast:	n/a
25	chr3:155480645-155480695	HCPEpiC	choroid plexus:	n/a
26	chr3:155480645-155480695	AG04450	lung:	fetal
27	chr3:155480645-155480695	SK-N-SH	brain:	n/a
28	chr3:155480645-155480695	CMK	blood:	n/a
29	chr3:155480645-155480695	BJ	skin:	n/a
30	chr3:155480645-155480695	HAEpiC	amniotic membrane:	n/a
31	chr3:155480645-155480695	NHBE	bronchial:	n/a
32	chr3:155480645-155480695	HIPEpiC	eye:	n/a
33	chr3:155480645-155480695	ovcar-3	ovarian:	n/a
34	chr3:155480645-155480695	H1-hESC	embryonic stem cell:	embryo
35	chr3:155480645-155480695	RPTEC	kidney:	n/a
36	chr3:155480645-155480695	HUVEC	blood vessel:	n/a
37	chr3:155480645-155480695	NB4	blood:	n/a
38	chr3:155480645-155480695	GM12892	blood:	n/a
39	chr3:155480645-155480695	AG10803	skin:	n/a
40	chr3:155480645-155480695	HCF	heart:	n/a
41	chr3:155480645-155480695	HepG2	liver:	n/a
42	chr3:155480645-155480695	MCF10A-Er-Src	breast:	n/a
43	chr3:155480645-155480695	NH-A	brain:	n/a
44	chr3:155480645-155480695	Caco-2	colon:	n/a
45	chr3:155480645-155480695	HNPCEpiC	eye:	n/a
46	chr3:155480645-155480695	SK-N-SH_RA	brain:	n/a
47	chr3:155480645-155480695	AoSMC	blood vessel:	n/a
48	chr3:155480645-155480695	SAEC	small airway:	n/a
49	chr3:155480645-155480695	HEK293	kidney:	embryo
50	chr3:155480645-155480695	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:155489353..155491545-chr3:155498387..155500105,2	MCF-7	breast:
2	chr3:155479593..155481988-chr3:155483221..155485642,3	K562	blood:
3	chr3:155491831..155494360-chr3:155588180..155590433,3	K562	blood:
4	chr3:155477418..155480054-chr3:155586699..155588871,2	MCF-7	breast:
5	chr3:155491839..155493601-chr3:155495108..155496890,2	K562	blood:
6	chr3:155483233..155486124-chr3:155587848..155589390,2	MCF-7	breast:
7	chr3:155489809..155491892-chr3:155496902..155499266,2	K562	blood:
8	chr3:155481429..155485286-chr3:155486373..155491702,5	K562	blood:
9	chr3:155476567..155478417-chr3:155522248..155524245,2	MCF-7	breast:
10	chr3:155480147..155483683-chr3:155487368..155490043,3	K562	blood:
11	chr3:155479593..155481988-chr3:155483221..155485642,3	K562	blood:
12	chr3:155475971..155478376-chr3:155587732..155590081,2	K562	blood:
13	chr3:155481429..155485286-chr3:155486373..155491702,5	K562	blood:
14	chr3:155468097..155470070-chr3:155473602..155476572,2	K562	blood:
15	chr3:155488449..155490862-chr3:155570678..155572291,2	MCF-7	breast:
16	chr3:155371134..155373846-chr3:155480180..155482982,2	K562	blood:
17	chr3:155480147..155483683-chr3:155487368..155490043,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf33-1	chr3:155474205-155475125	l_2508_chr3:155472774-155475125_lung
2	lnc-GMPS-3	chr3:155478406-155479006	NONHSAT092842

Variant related genes	Relation type
ENSG00000241307	TF binding region
ENSG00000241307	CpG island
ENSG00000169359	chromatin interactions
ENSG00000174928	chromatin interactions
ENSG00000163655	chromatin interactions

Extended variants
information (count: 743 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9811107	chr3:155474879-155474880	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184247999	chr3:155474883-155474884	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs538505791	chr3:155474935-155474936	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs188079790	chr3:155474945-155474946	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs139228040	chr3:155474961-155474962	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs59786750	chr3:155475008-155475009	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs554163464	chr3:155475027-155475028	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs575595046	chr3:155475037-155475038	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs79517979	chr3:155475045-155475046	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs564591350	chr3:155475076-155475077	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs111258866	chr3:155475092-155475093	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs541303090	chr3:155475102-155475103	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs143173293	chr3:155475116-155475117	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs530350332	chr3:155475122-155475123	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs371518231	chr3:155475123-155475124	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs9866823	chr3:155475157-155475158	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs148573046	chr3:155475166-155475167	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs142805039	chr3:155475169-155475170	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs150612009	chr3:155475203-155475204	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs140093445	chr3:155475224-155475225	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs143681040	chr3:155475263-155475264	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs565837306	chr3:155475285-155475286	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs192659906	chr3:155475295-155475296	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs184502975	chr3:155475324-155475325	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs73156600	chr3:155475352-155475353	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs536694131	chr3:155475382-155475383	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs558119702	chr3:155475385-155475386	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs201396610	chr3:155475403-155475404	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200231154	chr3:155475417-155475418	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs368144058	chr3:155475420-155475421	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs534370731	chr3:155475422-155475423	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs114642907	chr3:155475423-155475424	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs374136038	chr3:155475424-155475425	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs400999	chr3:155475463-155475464	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs542546081	chr3:155475506-155475507	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs564021121	chr3:155475513-155475514	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs116001291	chr3:155475580-155475581	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs370830812	chr3:155475582-155475583	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs146807149	chr3:155475620-155475621	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs190454089	chr3:155475642-155475643	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs547035440	chr3:155475679-155475680	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs565742973	chr3:155475686-155475687	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs35507021	chr3:155475696-155475697	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs181907255	chr3:155475737-155475738	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs34170786	chr3:155475748-155475749	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs73156602	chr3:155475756-155475757	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs569654659	chr3:155475763-155475764	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs540930918	chr3:155475798-155475799	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs558291755	chr3:155475807-155475808	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs184227996	chr3:155475810-155475811	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
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
head and neck squamous cell carcinoma	17671120	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
Breast cancer	21364760	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Cancer	17440070	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21611746	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155463800-155475200	Weak transcription	Left Ventricle	heart
2	chr3:155463800-155487800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:155463800-155501200	Weak transcription	Aorta	Aorta
4	chr3:155464000-155476600	Weak transcription	Ovary	ovary
5	chr3:155464200-155487600	Weak transcription	Brain Hippocampus Middle	brain
6	chr3:155464200-155487600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr3:155464200-155487800	Weak transcription	Adipose Nuclei	Adipose
8	chr3:155464200-155487800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr3:155464200-155487800	Weak transcription	Pancreas	Pancrea
10	chr3:155464200-155489600	Weak transcription	Brain Anterior Caudate	brain
11	chr3:155464200-155490600	Weak transcription	Stomach Smooth Muscle	stomach
12	chr3:155464600-155487800	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr3:155466400-155484600	Weak transcription	Fetal Brain Male	brain
14	chr3:155467000-155487200	Weak transcription	Fetal Brain Female	brain
15	chr3:155467200-155478400	Weak transcription	Fetal Intestine Large	intestine
16	chr3:155467200-155479400	Weak transcription	Fetal Intestine Small	intestine
17	chr3:155467200-155500200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:155467200-155508000	Weak transcription	K562	blood
19	chr3:155467200-155508800	Weak transcription	Hela-S3	cervix
20	chr3:155467400-155481600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:155467400-155508400	Weak transcription	HepG2	liver
22	chr3:155468000-155487200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr3:155469400-155481600	Weak transcription	Liver	Liver
24	chr3:155470000-155478800	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr3:155470200-155483000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr3:155470400-155487400	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr3:155470400-155487600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr3:155470800-155487400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr3:155471000-155481400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:155471000-155487400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr3:155471000-155487800	Weak transcription	Right Ventricle	heart
32	chr3:155471200-155487600	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr3:155471400-155509000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr3:155471800-155487600	Weak transcription	Brain Angular Gyrus	brain
35	chr3:155472200-155487600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr3:155472400-155487200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:155472800-155488000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:155472800-155500000	Weak transcription	Brain Cingulate Gyrus	brain
39	chr3:155473200-155487400	Weak transcription	Fetal Muscle Leg	muscle
40	chr3:155473200-155487400	Weak transcription	Thymus	Thymus
41	chr3:155474200-155487600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr3:155474200-155487800	Weak transcription	Spleen	Spleen
43	chr3:155474200-155490600	Weak transcription	Colon Smooth Muscle	Colon
44	chr3:155474200-155497600	Weak transcription	Fetal Muscle Trunk	muscle
45	chr3:155474400-155492000	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr3:155474800-155476600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr3:155474800-155487400	Weak transcription	Dnd41	blood
48	chr3:155474800-155487800	Weak transcription	Primary T cells from cord blood	blood
49	chr3:155474800-155489000	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr3:155475200-155476400	Strong transcription	Left Ventricle	heart

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