Variant report

Variant	nsv965394
Chromosome Location	chr3:119032370-119038786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr3:119037932-119038114	K562	blood:	n/a	n/a
2	CEBPB	chr3:119034573-119034701	HepG2	liver:	n/a	chr3:119034622-119034633 chr3:119034624-119034635
3	CEBPB	chr3:119034465-119034797	IMR90	lung:	n/a	chr3:119034622-119034633 chr3:119034624-119034635
4	CUX1	chr3:119032203-119032441	K562	blood:	n/a	n/a
5	EP300	chr3:119033699-119033957	SK-N-SH_RA	brain:	n/a	n/a
6	EP300	chr3:119037815-119038171	SK-N-SH_RA	brain:	n/a	n/a
7	EP300	chr3:119033665-119034019	SK-N-SH_RA	brain:	n/a	n/a
8	EP300	chr3:119037794-119038109	SK-N-SH_RA	brain:	n/a	n/a
9	EP300	chr3:119033112-119034753	SK-N-SH	brain:	n/a	n/a
10	GATA1	chr3:119037836-119038588	PBDE	blood:	n/a	chr3:119038323-119038339 chr3:119038326-119038335
11	GATA3	chr3:119037721-119038608	SK-N-SH	brain:	n/a	chr3:119038323-119038339 chr3:119038326-119038335
12	GATA3	chr3:119037852-119038072	SH-SY5Y	brain:	n/a	n/a
13	GTF2F1	chr3:119036634-119036635	K562	blood:	n/a	n/a
14	MAFK	chr3:119035682-119035872	HepG2	liver:	n/a	chr3:119035727-119035741 chr3:119035724-119035739
15	MAFK	chr3:119035611-119035882	HepG2	liver:	n/a	chr3:119035727-119035741 chr3:119035724-119035739
16	POLR2A	chr3:119033628-119033740	MCF10A-Er-Src	breast:	n/a	n/a
17	POLR2A	chr3:119034696-119034783	MCF10A-Er-Src	breast:	n/a	n/a
18	POLR2A	chr3:119034887-119034992	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr3:119037775-119038122	SK-N-SH	brain:	n/a	n/a
20	POLR2A	chr3:119038291-119038357	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr3:119033430-119033476	HUVEC	blood vessel:	n/a	n/a
22	RCOR1	chr3:119034857-119035117	K562	blood:	n/a	n/a
23	RCOR1	chr3:119037876-119038048	K562	blood:	n/a	n/a
24	REST	chr3:119034420-119034698	SK-N-SH	brain:	n/a	n/a
25	SPI1	chr3:119032812-119033020	GM12891	blood:	n/a	n/a
26	SPI1	chr3:119032892-119033059	K562	blood:	n/a	n/a
27	STAT3	chr3:119034774-119034817	MCF10A-Er-Src	breast:	n/a	n/a
28	STAT3	chr3:119037069-119037181	MCF10A-Er-Src	breast:	n/a	n/a
29	TCF12	chr3:119037618-119038342	SK-N-SH	brain:	n/a	n/a
30	TCF12	chr3:119037644-119038327	SK-N-SH	brain:	n/a	n/a
31	UBTF	chr3:119033284-119033438	K562	blood:	n/a	n/a
32	USF1	chr3:119034890-119035144	SK-N-SH_RA	brain:	n/a	n/a
33	USF1	chr3:119034782-119035102	A549	lung:	n/a	n/a
34	USF2	chr3:119034982-119034997	Hela-S3	cervix:	n/a	n/a
35	USF2	chr3:119034947-119035000	HepG2	liver:	n/a	chr3:119034980-119034991
36	ZNF384	chr3:119037871-119038143	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:119038549-119038599	HCM	heart:	n/a
2	chr3:119038549-119038599	H1-hESC	embryonic stem cell:	embryo
3	chr3:119038549-119038599	PrEC	prostate:	n/a
4	chr3:119038549-119038599	HEK293	kidney:	embryo
5	chr3:119038549-119038599	HPAEpiC	pulmonary alveolar:	n/a
6	chr3:119038549-119038599	NT2-D1	testis:	n/a
7	chr3:119038549-119038599	IMR90	lung:	fetal
8	chr3:119038549-119038599	BJ	skin:	n/a
9	chr3:119038549-119038599	CMK	blood:	n/a
10	chr3:119038549-119038599	PANC-1	pancreas:	n/a
11	chr3:119038549-119038599	AG10803	skin:	n/a
12	chr3:119038549-119038599	NB4	blood:	n/a
13	chr3:119038549-119038599	BE2_C	brain:	n/a
14	chr3:119038549-119038599	HIPEpiC	eye:	n/a
15	chr3:119038549-119038599	GM12891	blood:	n/a
16	chr3:119038549-119038599	Jurkat	blood:	n/a
17	chr3:119038549-119038599	GM12892	blood:	n/a
18	chr3:119038549-119038599	SK-N-SH_RA	brain:	n/a
19	chr3:119038549-119038599	HL-60	blood:	n/a
20	chr3:119038549-119038599	MCF-7	breast:	n/a
21	chr3:119038549-119038599	AG09309	skin:	n/a
22	chr3:119038549-119038599	U87	brain:	n/a
23	chr3:119038549-119038599	Hepatocyte	liver:	n/a
24	chr3:119038549-119038599	SKMC	muscle:	n/a
25	chr3:119038549-119038599	HMEC	breast:	n/a
26	chr3:119038549-119038599	GM06990	blood:	n/a
27	chr3:119038549-119038599	Hela-S3	cervix:	n/a
28	chr3:119038549-119038599	HUVEC	blood vessel:	n/a
29	chr3:119038549-119038599	HEEpiC	esophagus:	n/a
30	chr3:119038549-119038599	NHBE	bronchial:	n/a
31	chr3:119038549-119038599	AG04449	skin:	fetal
32	chr3:119038549-119038599	Caco-2	colon:	n/a
33	chr3:119038549-119038599	A549	lung:	n/a
34	chr3:119038549-119038599	SK-N-MC	brain:	n/a
35	chr3:119038549-119038599	SAEC	small airway:	n/a
36	chr3:119038549-119038599	HCF	heart:	n/a
37	chr3:119038549-119038599	NHDF-neo	bronchial:	n/a
38	chr3:119038549-119038599	AG04450	lung:	fetal
39	chr3:119038549-119038599	ECC-1	luminal epithelium:	n/a
40	chr3:119038549-119038599	HepG2	liver:	n/a
41	chr3:119038549-119038599	GM12878	blood:	n/a
42	chr3:119038549-119038599	GM19239	blood:	n/a
43	chr3:119038549-119038599	HAEpiC	amniotic membrane:	n/a
44	chr3:119038549-119038599	LNCaP	prostate:	n/a
45	chr3:119038549-119038599	RPTEC	kidney:	n/a
46	chr3:119038549-119038599	NH-A	brain:	n/a
47	chr3:119038549-119038599	ProgFib	skin:	n/a
48	chr3:119038549-119038599	HRPEpiC	eye:	n/a
49	chr3:119038549-119038599	K562	blood:	n/a
50	chr3:119038549-119038599	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:119011664..119014581-chr3:119029307..119032629,3	MCF-7	breast:
2	chr3:119032938..119036654-chr3:119043766..119046984,5	MCF-7	breast:
3	chr3:118969877..118972068-chr3:119030685..119033173,2	K562	blood:
4	chr3:119009764..119012007-chr3:119036606..119039583,2	MCF-7	breast:
5	chr3:119034010..119039174-chr3:119039543..119045383,10	K562	blood:
6	chr3:119016211..119028042-chr3:119037960..119043695,12	MCF-7	breast:
7	chr3:118958216..118961289-chr3:119031981..119034606,3	K562	blood:
8	chr3:119032410..119034718-chr3:119043849..119046722,2	K562	blood:
9	chr3:119028893..119037158-chr3:119037697..119043591,18	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B4GALT4-1	chr3:119033140-119033616	ENSG00000241155.1

No data

Variant related genes	Relation type
ARHGAP31	TF binding region
ARHGAP31	CpG island
ENSG00000031081	chromatin interactions
ENSG00000241155	chromatin interactions
ENSG00000242829	chromatin interactions
ENSG00000121578	chromatin interactions

Extended variants
information (count: 216 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:216 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115344098	chr3:119032426-119032427	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs76930289	chr3:119032448-119032449	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs561786058	chr3:119032457-119032458	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs149885309	chr3:119032458-119032459	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs554593865	chr3:119032512-119032513	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs376207133	chr3:119032539-119032540	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs6799733	chr3:119032547-119032548	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs142410355	chr3:119032548-119032549	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs553598902	chr3:119032588-119032589	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs540594486	chr3:119032678-119032679	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs187949140	chr3:119032770-119032771	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs192189733	chr3:119032795-119032796	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs145969568	chr3:119032817-119032818	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs557144315	chr3:119032821-119032822	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs184398200	chr3:119032830-119032831	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs9872394	chr3:119032872-119032873	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs561494232	chr3:119032879-119032880	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs371438269	chr3:119032895-119032896	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs116789121	chr3:119032932-119032933	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376169651	chr3:119032965-119032966	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs75023168	chr3:119032992-119032993	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs570644684	chr3:119033012-119033013	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs139829777	chr3:119033130-119033131	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs532956648	chr3:119033139-119033140	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs9834750	chr3:119033157-119033158	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs141505423	chr3:119033174-119033175	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs569111027	chr3:119033207-119033208	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs529809339	chr3:119033208-119033209	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs548330165	chr3:119033226-119033227	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs188079789	chr3:119033326-119033327	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs533756387	chr3:119033363-119033364	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs558273763	chr3:119033373-119033374	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs571872069	chr3:119033405-119033406	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs538989179	chr3:119033416-119033417	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs71325374	chr3:119033420-119033421	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs557130196	chr3:119033426-119033427	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs191656610	chr3:119033438-119033439	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs144849907	chr3:119033509-119033510	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs566643078	chr3:119033515-119033516	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs555013129	chr3:119033561-119033562	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs573278049	chr3:119033569-119033570	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs540574099	chr3:119033579-119033580	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs375286379	chr3:119033585-119033586	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs74600686	chr3:119033586-119033587	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs148576367	chr3:119033614-119033615	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs75397941	chr3:119033623-119033624	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs562648935	chr3:119033683-119033684	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs560493650	chr3:119033685-119033686	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs529947748	chr3:119033744-119033745	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs548428361	chr3:119033747-119033748	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 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
High-grade prostatic intraepithelial neoplasia	16573809	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119014200-119032800	Weak transcription	Pancreas	Pancrea
2	chr3:119015000-119041200	Weak transcription	Aorta	Aorta
3	chr3:119015200-119041000	Weak transcription	Fetal Kidney	kidney
4	chr3:119016000-119035400	Weak transcription	Fetal Brain Male	brain
5	chr3:119016000-119041000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr3:119016400-119040800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr3:119016400-119041000	Weak transcription	Fetal Intestine Small	intestine
8	chr3:119017400-119040600	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr3:119017600-119032400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr3:119018800-119032800	Weak transcription	Thymus	Thymus
11	chr3:119019200-119040800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr3:119020400-119040600	Weak transcription	Esophagus	oesophagus
13	chr3:119020800-119032400	Weak transcription	Fetal Muscle Trunk	muscle
14	chr3:119021000-119032400	Weak transcription	Primary T cells from cord blood	blood
15	chr3:119021200-119041000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr3:119021200-119041000	Weak transcription	Fetal Thymus	thymus
17	chr3:119022000-119032400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr3:119022200-119040800	Weak transcription	Brain Angular Gyrus	brain
19	chr3:119022400-119040600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr3:119022400-119041000	Weak transcription	Primary B cells from cord blood	blood
21	chr3:119022400-119041000	Weak transcription	Fetal Intestine Large	intestine
22	chr3:119022400-119041200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr3:119022600-119032600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr3:119022600-119040600	Weak transcription	Primary B cells from peripheral blood	blood
25	chr3:119023600-119032800	Weak transcription	Ovary	ovary
26	chr3:119024400-119040600	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr3:119024800-119032400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr3:119024800-119032600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr3:119024800-119032800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr3:119024800-119040600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr3:119024800-119041000	Weak transcription	Colon Smooth Muscle	Colon
32	chr3:119024800-119041000	Weak transcription	Rectal Smooth Muscle	rectum
33	chr3:119025000-119040800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr3:119026800-119034600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr3:119027600-119033800	Weak transcription	Brain Substantia Nigra	brain
36	chr3:119027600-119041000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr3:119028200-119032800	Weak transcription	Fetal Muscle Leg	muscle
38	chr3:119029200-119032400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr3:119029400-119039000	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr3:119029600-119033000	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr3:119029600-119041200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:119029800-119033200	Strong transcription	Cortex derived primary cultured neurospheres	brain
43	chr3:119030000-119041000	Weak transcription	Brain Anterior Caudate	brain
44	chr3:119030000-119041200	Weak transcription	Gastric	stomach
45	chr3:119030200-119038800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr3:119030200-119041000	Weak transcription	Colonic Mucosa	Colon
47	chr3:119030400-119032400	Weak transcription	Right Ventricle	heart
48	chr3:119030600-119032400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr3:119030600-119032400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr3:119030600-119032400	Weak transcription	Fetal Stomach	stomach

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