Variant report

Variant	nsv878143
Chromosome Location	chr3:195115229-195158031
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:158)
CpG islands
(count:0)
Chromatin interactive
region (count:41)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:158 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:195118576-195118596	K562	blood:	n/a	n/a
2	ATF1	chr3:195146585-195147032	K562	blood:	n/a	n/a
3	CEBPB	chr3:195142195-195142415	HepG2	liver:	n/a	n/a
4	CEBPB	chr3:195116091-195116306	HepG2	liver:	n/a	n/a
5	CEBPB	chr3:195117681-195117825	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr3:195134221-195134401	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:195134115-195134423	HepG2	liver:	n/a	n/a
8	CEBPB	chr3:195134135-195134369	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:195137594-195137784	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:195117516-195117880	K562	blood:	n/a	n/a
11	CEBPB	chr3:195117387-195117882	IMR90	lung:	n/a	n/a
12	CEBPB	chr3:195142168-195142509	IMR90	lung:	n/a	n/a
13	CEBPB	chr3:195133956-195134439	MCF-7	breast:	n/a	chr3:195134040-195134053
14	CEBPB	chr3:195141077-195141184	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr3:195134115-195134473	A549	lung:	n/a	n/a
16	CEBPB	chr3:195134103-195134474	K562	blood:	n/a	n/a
17	CEBPB	chr3:195142185-195142500	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr3:195146731-195146822	K562	blood:	n/a	n/a
19	CEBPB	chr3:195134080-195134538	MCF-7	breast:	n/a	n/a
20	CEBPB	chr3:195133940-195134434	IMR90	lung:	n/a	chr3:195134040-195134053
21	CEBPB	chr3:195134110-195134480	K562	blood:	n/a	n/a
22	CTCF	chr3:195142020-195142170	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr3:195127764-195127815	GM13976	blood:	n/a	n/a
24	CTCF	chr3:195116791-195116829	GM20000	blood:	n/a	n/a
25	CTCF	chr3:195146880-195147030	NHEK	skin:	n/a	n/a
26	CTCF	chr3:195116280-195116430	GM12872	blood:	n/a	n/a
27	CUX1	chr3:195117710-195117743	GM12878	blood:	n/a	n/a
28	E2F4	chr3:195139915-195139987	MCF10A-Er-Src	breast:	n/a	n/a
29	EBF1	chr3:195130536-195130817	GM12878	blood:	n/a	chr3:195130671-195130682
30	EBF1	chr3:195130658-195130846	GM12878	blood:	n/a	chr3:195130671-195130682
31	ELK1	chr3:195127553-195127590	GM12878	blood:	n/a	n/a
32	ELK1	chr3:195116026-195116034	GM12878	blood:	n/a	n/a
33	EP300	chr3:195122472-195123263	SK-N-SH	brain:	n/a	n/a
34	EP300	chr3:195122744-195122988	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr3:195146642-195146851	K562	blood:	n/a	n/a
36	FAM48A	chr3:195146643-195146729	GM12878	blood:	n/a	n/a
37	FOS	chr3:195146975-195147142	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr3:195142189-195142513	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr3:195142263-195142414	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr3:195142192-195142531	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr3:195147070-195147124	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr3:195117381-195117790	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr3:195137547-195137892	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr3:195142169-195142504	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:195117395-195117819	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr3:195137510-195137907	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr3:195137503-195137892	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr3:195137541-195137900	MCF10A-Er-Src	breast:	n/a	n/a
49	FOSL1	chr3:195137468-195137890	HCT-116	colon:	n/a	n/a
50	FOSL1	chr3:195137418-195137977	HCT-116	colon:	n/a	n/a

No data

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195146199..195148452-chr3:195160280..195163099,3	K562	blood:
2	chr3:195137797..195139503-chr3:195140426..195142233,2	K562	blood:
3	chr3:195115819..195117385-chr3:195118245..195120989,2	K562	blood:
4	chr3:195140841..195144562-chr3:195162186..195164822,3	K562	blood:
5	chr3:195151499..195154250-chr3:195155188..195159496,5	K562	blood:
6	chr3:195140418..195142726-chr3:195147960..195149688,2	K562	blood:
7	chr3:195140418..195142726-chr3:195147960..195149688,2	K562	blood:
8	chr3:195155869..195158783-chr3:195162200..195163849,3	MCF-7	breast:
9	chr3:195118577..195121196-chr3:195123610..195125221,2	K562	blood:
10	chr3:195107747..195110594-chr3:195131187..195133391,2	MCF-7	breast:
11	chr3:195118577..195121196-chr3:195123610..195125221,2	K562	blood:
12	chr3:195112021..195114749-chr3:195120473..195123237,3	K562	blood:
13	chr3:195145080..195147347-chr3:195150908..195152978,2	K562	blood:
14	chr3:195145480..195148513-chr3:195161599..195165057,3	K562	blood:
15	chr3:195149095..195152124-chr3:195158783..195163534,4	MCF-7	breast:
16	chr3:195147386..195148942-chr3:195155792..195158079,2	MCF-7	breast:
17	chr3:195145080..195147347-chr3:195150908..195152978,2	K562	blood:
18	chr3:195150893..195158887-chr3:195161492..195167356,11	K562	blood:
19	chr3:195138714..195141452-chr3:195144940..195147582,4	K562	blood:
20	chr3:195151499..195154250-chr3:195155188..195159496,5	K562	blood:
21	chr3:195139973..195142726-chr3:195146764..195149688,2	K562	blood:
22	chr3:195137707..195139591-chr3:195140470..195142903,2	MCF-7	breast:
23	chr3:195127749..195130256-chr3:195162538..195164102,2	K562	blood:
24	chr3:195115819..195117385-chr3:195118245..195120989,2	K562	blood:
25	chr3:195118569..195121497-chr3:195125322..195127616,3	K562	blood:
26	chr3:195137707..195139591-chr3:195140470..195142903,2	MCF-7	breast:
27	chr3:195114422..195115970-chr3:195117512..195119641,2	MCF-7	breast:
28	chr3:195152582..195154526-chr3:195161625..195163780,3	K562	blood:
29	chr3:195109170..195110798-chr3:195111996..195115917,3	K562	blood:
30	chr3:195112021..195114913-chr3:195121737..195123934,2	K562	blood:
31	chr3:195139843..195142071-chr3:195162223..195164874,2	MCF-7	breast:
32	chr3:195108508..195110798-chr3:195111996..195115917,4	K562	blood:
33	chr3:195152779..195154771-chr3:195162258..195164678,3	MCF-7	breast:
34	chr3:195147386..195148942-chr3:195155792..195158079,2	MCF-7	breast:
35	chr3:195140758..195142761-chr3:195162316..195165010,2	MCF-7	breast:
36	chr3:195118569..195121497-chr3:195125322..195127616,3	K562	blood:
37	chr3:195086495..195088641-chr3:195116660..195118594,2	K562	blood:
38	chr3:195131548..195133612-chr3:195139507..195142026,2	K562	blood:
39	chr3:195137797..195139503-chr3:195140426..195142233,2	K562	blood:
40	chr3:195106101..195107795-chr3:195127208..195129590,2	MCF-7	breast:
41	chr3:195114422..195115970-chr3:195117512..195119641,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACAP2-1	chr3:195157857-195159161	refGeneNc_4303_NR_033944

No data

Variant related genes	Relation type
ENSG00000207368	TF binding region
ENSG00000207368	chromatin interactions
ENSG00000114331	chromatin interactions

Extended variants
information (count: 1624 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1624 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542723666	chr3:195115294-195115295	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs188819194	chr3:195115303-195115304	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs533133104	chr3:195115306-195115307	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs60222890	chr3:195115311-195115312	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs570122342	chr3:195115358-195115359	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs537090932	chr3:195115370-195115371	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs566994042	chr3:195115382-195115383	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs192821113	chr3:195115442-195115443	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs562428448	chr3:195115485-195115486	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs139429713	chr3:195115517-195115518	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs553215071	chr3:195115611-195115612	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs117821346	chr3:195115630-195115631	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs369447640	chr3:195115632-195115633	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs73080815	chr3:195115640-195115641	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs569493834	chr3:195115646-195115647	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs57869834	chr3:195115647-195115648	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs80195578	chr3:195115649-195115650	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs557473719	chr3:195115660-195115661	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs397959961	chr3:195115664-195115665	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs62288366	chr3:195115668-195115669	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs575732710	chr3:195115746-195115747	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs184915423	chr3:195115764-195115765	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs561709845	chr3:195115774-195115775	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs573523323	chr3:195115798-195115799	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs78089179	chr3:195115812-195115813	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs533168852	chr3:195115831-195115832	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs570542535	chr3:195115834-195115835	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs189342628	chr3:195115870-195115871	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs79011172	chr3:195115898-195115899	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs142587738	chr3:195115910-195115911	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs540886167	chr3:195115961-195115962	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs531011468	chr3:195116016-195116017	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74289303	chr3:195116029-195116030	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567665155	chr3:195116033-195116034	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371599829	chr3:195116084-195116085	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370574421	chr3:195116142-195116143	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528445687	chr3:195116152-195116153	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139893902	chr3:195116192-195116193	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs823309	chr3:195116255-195116256	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs531365340	chr3:195116268-195116269	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538895780	chr3:195116286-195116287	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568212313	chr3:195116303-195116304	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs180923021	chr3:195116332-195116333	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183911788	chr3:195116355-195116356	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189169089	chr3:195116366-195116367	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7429738	chr3:195116506-195116507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149812694	chr3:195116566-195116567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573586657	chr3:195116591-195116592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540985858	chr3:195116592-195116593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553343139	chr3:195116593-195116594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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	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
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195041000-195131200	Weak transcription	Gastric	stomach
2	chr3:195052400-195118000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr3:195074800-195118000	Weak transcription	K562	blood
4	chr3:195077400-195118000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr3:195077800-195117800	Weak transcription	Brain Angular Gyrus	brain
6	chr3:195077800-195122800	Weak transcription	Right Ventricle	heart
7	chr3:195078000-195142200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr3:195078600-195118000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr3:195087800-195131200	Weak transcription	NHDF-Ad	bronchial
10	chr3:195088600-195146800	Weak transcription	Spleen	Spleen
11	chr3:195090800-195116800	Weak transcription	Aorta	Aorta
12	chr3:195091400-195116200	Weak transcription	Liver	Liver
13	chr3:195094800-195161200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr3:195095200-195116800	Weak transcription	Fetal Muscle Trunk	muscle
15	chr3:195095200-195161800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr3:195095800-195134200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:195100600-195117000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr3:195101800-195122200	Weak transcription	Primary hematopoietic stem cells	blood
19	chr3:195102600-195115400	Weak transcription	Adipose Nuclei	Adipose
20	chr3:195102600-195118000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr3:195102600-195129800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr3:195102800-195115400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:195103800-195117400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr3:195105400-195115400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr3:195106000-195118000	Weak transcription	Small Intestine	intestine
26	chr3:195106600-195117600	Weak transcription	NHLF	lung
27	chr3:195106600-195118000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:195106600-195137800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr3:195106800-195117800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr3:195106800-195117800	Weak transcription	Brain Anterior Caudate	brain
31	chr3:195107000-195115400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr3:195107000-195116800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr3:195107000-195118000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr3:195107000-195119400	Weak transcription	HSMM	muscle
35	chr3:195107400-195126600	Weak transcription	Esophagus	oesophagus
36	chr3:195107800-195115400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr3:195107800-195118000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr3:195108800-195134000	Weak transcription	Placenta	Placenta
39	chr3:195109200-195118000	Weak transcription	Duodenum Mucosa	Duodenum
40	chr3:195109400-195117800	Weak transcription	Fetal Lung	lung
41	chr3:195109400-195118000	Weak transcription	Stomach Mucosa	stomach
42	chr3:195109400-195144000	Weak transcription	Fetal Muscle Leg	muscle
43	chr3:195109800-195131200	Weak transcription	Fetal Intestine Large	intestine
44	chr3:195111400-195121200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr3:195111800-195115400	Weak transcription	Fetal Thymus	thymus
46	chr3:195111800-195128400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr3:195112400-195123800	Weak transcription	Left Ventricle	heart
48	chr3:195112400-195126600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr3:195112600-195118000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr3:195112600-195121400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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