Variant report

Variant	nsv876593
Chromosome Location	chr3:17419843-17604963
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1427)
CpG islands
(count:0)
Chromatin interactive
region (count:91)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1427 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:17506407-17506512	K562	blood:	n/a	n/a
2	ARID3A	chr3:17484122-17484922	K562	blood:	n/a	n/a
3	ARID3A	chr3:17462080-17462754	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:17472416-17472770	K562	blood:	n/a	n/a
5	ARID3A	chr3:17454500-17454738	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:17486399-17486776	K562	blood:	n/a	n/a
7	ATF1	chr3:17520229-17520516	K562	blood:	n/a	n/a
8	ATF1	chr3:17472550-17472822	K562	blood:	n/a	n/a
9	ATF1	chr3:17484018-17484387	K562	blood:	n/a	n/a
10	ATF1	chr3:17486434-17486698	K562	blood:	n/a	n/a
11	ATF1	chr3:17484669-17484932	K562	blood:	n/a	n/a
12	ATF1	chr3:17594526-17594848	K562	blood:	n/a	n/a
13	ATF2	chr3:17440604-17441083	GM12878	blood:	n/a	n/a
14	ATF2	chr3:17440529-17441152	GM12878	blood:	n/a	n/a
15	ATF3	chr3:17484214-17484440	K562	blood:	n/a	n/a
16	ATF3	chr3:17486331-17486754	K562	blood:	n/a	n/a
17	ATF3	chr3:17484191-17484365	K562	blood:	n/a	n/a
18	ATF3	chr3:17520058-17520526	A549	lung:	n/a	n/a
19	ATF3	chr3:17520011-17520619	A549	lung:	n/a	n/a
20	BACH1	chr3:17473755-17474077	H1-hESC	embryonic stem cell:	n/a	chr3:17473906-17473920
21	BACH1	chr3:17474299-17474445	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr3:17473751-17474065	K562	blood:	n/a	chr3:17473906-17473920
23	BACH1	chr3:17539622-17539654	K562	blood:	n/a	n/a
24	BATF	chr3:17593881-17594130	GM12878	blood:	n/a	n/a
25	BATF	chr3:17440687-17441050	GM12878	blood:	n/a	n/a
26	BATF	chr3:17440584-17441027	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:17440636-17441099	GM12878	blood:	n/a	chr3:17440792-17440801
28	BCL11A	chr3:17440655-17441034	GM12878	blood:	n/a	chr3:17440792-17440801
29	BCL3	chr3:17556772-17557520	A549	lung:	n/a	n/a
30	BCL3	chr3:17520027-17520714	A549	lung:	n/a	n/a
31	BCLAF1	chr3:17440619-17441234	GM12878	blood:	n/a	chr3:17440792-17440801
32	BCLAF1	chr3:17440538-17441322	GM12878	blood:	n/a	chr3:17440792-17440801
33	BHLHE40	chr3:17520199-17520344	HepG2	liver:	n/a	n/a
34	BHLHE40	chr3:17484668-17485011	K562	blood:	n/a	n/a
35	BHLHE40	chr3:17428087-17428202	K562	blood:	n/a	n/a
36	BHLHE40	chr3:17462222-17462436	K562	blood:	n/a	n/a
37	BHLHE40	chr3:17462223-17462521	HepG2	liver:	n/a	n/a
38	BHLHE40	chr3:17440644-17441042	GM12878	blood:	n/a	n/a
39	BRCA1	chr3:17454624-17454755	HepG2	liver:	n/a	n/a
40	BRCA1	chr3:17519940-17520632	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr3:17556814-17557449	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr3:17484569-17485167	K562	blood:	n/a	n/a
43	CBX3	chr3:17484048-17484463	K562	blood:	n/a	n/a
44	CCNT2	chr3:17550451-17550562	K562	blood:	n/a	n/a
45	CCNT2	chr3:17549088-17549253	K562	blood:	n/a	n/a
46	CCNT2	chr3:17472494-17472658	K562	blood:	n/a	n/a
47	CEBPB	chr3:17486194-17486803	K562	blood:	n/a	n/a
48	CEBPB	chr3:17520018-17520830	A549	lung:	n/a	n/a
49	CEBPB	chr3:17475286-17475428	A549	lung:	n/a	n/a
50	CEBPB	chr3:17485633-17485949	K562	blood:	n/a	n/a

No data

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:17585640..17587263-chr3:17782584..17784641,2	MCF-7	breast:
2	chr3:17574853..17577476-chr3:17578727..17581379,2	K562	blood:
3	chr3:17419146..17421913-chr3:17422228..17424571,2	K562	blood:
4	chr3:17472134..17473149-chr3:17882441..17883393,5	K562	blood:
5	chr3:17484535..17486940-chr3:17491207..17493318,2	MCF-7	breast:
6	chr3:17590228..17593436-chr3:17593519..17596820,3	MCF-7	breast:
7	chr3:17561404..17563252-chr3:17564613..17567165,2	K562	blood:
8	chr3:17484813..17486609-chr3:17782332..17783917,2	MCF-7	breast:
9	chr3:17468044..17471008-chr3:17472912..17474863,2	MCF-7	breast:
10	chr3:17299624..17302842-chr3:17453304..17456180,3	MCF-7	breast:
11	chr3:17463709..17467146-chr3:17467192..17469844,3	K562	blood:
12	chr3:17454593..17456440-chr3:17885577..17887079,2	MCF-7	breast:
13	chr3:17300074..17301498-chr3:17454119..17455081,6	K562	blood:
14	chr3:17563803..17565634-chr3:17567663..17570561,2	K562	blood:
15	chr3:17514624..17515516-chr3:17727784..17728694,2	MCF-7	breast:
16	chr3:17552302..17553888-chr3:17553996..17555842,2	K562	blood:
17	chr3:17510239..17513029-chr3:190165164..190166664,2	MCF-7	breast:
18	chr3:17518313..17520629-chr3:17521648..17524012,2	MCF-7	breast:
19	chr3:17472375..17473059-chr3:17727721..17728808,3	MCF-7	breast:
20	chr3:17464487..17468576-chr3:17470106..17473767,3	K562	blood:
21	chr3:17471748..17472727-chr3:18430698..18431277,2	MCF-7	breast:
22	chr3:17415575..17418642-chr3:17419331..17422264,3	MCF-7	breast:
23	chr3:17472139..17473280-chr3:17881966..17883098,4	MCF-7	breast:
24	chr3:17497521..17499126-chr3:17503539..17506247,2	MCF-7	breast:
25	chr3:17299444..17301149-chr3:17449495..17452150,2	K562	blood:
26	chr3:17561404..17563252-chr3:17564613..17567165,2	K562	blood:
27	chr3:17426084..17429101-chr3:17432439..17434660,3	MCF-7	breast:
28	chr3:17599124..17601817-chr3:17607605..17609394,2	K562	blood:
29	chr3:17507187..17509434-chr3:17516355..17517975,2	MCF-7	breast:
30	chr3:17585835..17588259-chr3:17590207..17593064,3	K562	blood:
31	chr3:17472682..17474282-chr3:17477579..17479223,2	K562	blood:
32	chr3:17555908..17557459-chr3:17626910..17628494,2	K562	blood:
33	chr3:17348679..17349303-chr3:17454556..17455118,3	MCF-7	breast:
34	chr3:17300330..17301004-chr3:17455425..17455933,2	K562	blood:
35	chr3:17497865..17499392-chr3:17503466..17506313,2	K562	blood:
36	chr3:17348477..17349876-chr3:17454198..17455145,8	MCF-7	breast:
37	chr3:17463498..17465841-chr3:17880192..17882882,2	MCF-7	breast:
38	chr3:17585835..17588259-chr3:17590207..17593064,3	K562	blood:
39	chr3:17520321..17522399-chr3:17522640..17525341,2	K562	blood:
40	chr3:17472682..17474282-chr3:17477579..17479223,2	K562	blood:
41	chr3:17460223..17462241-chr3:17894481..17896425,2	K562	blood:
42	chr3:17422120..17423958-chr3:17425722..17427286,2	MCF-7	breast:
43	chr3:17472326..17472977-chr3:17727996..17728715,2	MCF-7	breast:
44	chr3:17484535..17486940-chr3:17491207..17493318,2	MCF-7	breast:
45	chr3:17468044..17471008-chr3:17472912..17474863,2	MCF-7	breast:
46	chr3:17466006..17468780-chr3:17782780..17784383,2	MCF-7	breast:
47	chr3:17515055..17515929-chr3:17882561..17883391,3	MCF-7	breast:
48	chr3:17422120..17423958-chr3:17425722..17427286,2	MCF-7	breast:
49	chr3:17455901..17458583-chr3:17462176..17465120,2	K562	blood:
50	chr3:17563803..17565634-chr3:17567663..17570561,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SATB1-8	chr3:17550041-17550097	NONHSAT088551
2	lnc-PLCL2-9	chr3:17567733-17568134	uc_483_+
3	lnc-PLCL2-8	chr3:17506642-17507002	NONHSAT088548
4	lnc-SATB1-7	chr3:17567733-17568134	uc_483_-

No data

Variant related genes	Relation type
ENSG00000227309	TF binding region
TBC1D5	TF binding region
ENSG00000131374	chromatin interactions

Extended variants
information (count: 6686 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:6686 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9848610	chr3:17419843-17419844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145212959	chr3:17419858-17419859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577246351	chr3:17419888-17419889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570828839	chr3:17419889-17419890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537454396	chr3:17419966-17419967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554218553	chr3:17419970-17419971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550496497	chr3:17419999-17420000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34191383	chr3:17420001-17420002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533923387	chr3:17420024-17420025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs137892379	chr3:17420025-17420026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372616913	chr3:17420072-17420073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545707480	chr3:17420079-17420080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559295992	chr3:17420143-17420144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575681662	chr3:17420201-17420202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532688270	chr3:17420259-17420260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202093055	chr3:17420260-17420261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544632251	chr3:17420269-17420270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538268932	chr3:17420305-17420306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561299791	chr3:17420310-17420311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556166429	chr3:17420311-17420312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140595792	chr3:17420327-17420328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540765921	chr3:17420473-17420474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150490559	chr3:17420505-17420506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs17043527	chr3:17420528-17420529	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs552008827	chr3:17420532-17420533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111229499	chr3:17420546-17420547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191250000	chr3:17420566-17420567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs143444968	chr3:17420586-17420587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184870913	chr3:17420617-17420618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568076316	chr3:17420644-17420645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533647185	chr3:17420645-17420646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553872594	chr3:17420650-17420651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528667076	chr3:17420655-17420656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs13077480	chr3:17420674-17420675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571918892	chr3:17420689-17420690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs17043529	chr3:17420702-17420703	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs61210790	chr3:17420730-17420731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs367776222	chr3:17420771-17420772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371747787	chr3:17420783-17420784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138272198	chr3:17420816-17420817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575991681	chr3:17420830-17420831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189152094	chr3:17420844-17420845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370787606	chr3:17420950-17420951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574813690	chr3:17420998-17420999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540325256	chr3:17421040-17421041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116945773	chr3:17421061-17421062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576936525	chr3:17421068-17421069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149625887	chr3:17421069-17421070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76837057	chr3:17421127-17421128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs143348265	chr3:17421132-17421133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	21364760	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1514 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:17339400-17442200	Weak transcription	Fetal Intestine Small	intestine
2	chr3:17344400-17439000	Weak transcription	Aorta	Aorta
3	chr3:17398800-17430200	Weak transcription	Pancreas	Pancrea
4	chr3:17398800-17447000	Weak transcription	Fetal Stomach	stomach
5	chr3:17401600-17432600	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr3:17402400-17443200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr3:17402600-17451000	Weak transcription	Gastric	stomach
8	chr3:17403000-17443000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr3:17403200-17449200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr3:17403400-17442200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr3:17404200-17449200	Weak transcription	Esophagus	oesophagus
12	chr3:17405000-17432400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr3:17406400-17442000	Weak transcription	Lung	lung
14	chr3:17407600-17443400	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr3:17409200-17430800	Weak transcription	Fetal Muscle Leg	muscle
16	chr3:17409200-17435000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr3:17410000-17426800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr3:17410200-17445200	Weak transcription	Right Ventricle	heart
19	chr3:17410200-17445600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr3:17410200-17447200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr3:17410200-17451400	Weak transcription	Brain Angular Gyrus	brain
22	chr3:17410400-17443400	Weak transcription	Brain Cingulate Gyrus	brain
23	chr3:17410400-17447800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:17411200-17467400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr3:17411600-17424000	Weak transcription	Spleen	Spleen
26	chr3:17411600-17425200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr3:17411600-17430800	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr3:17411600-17442000	Weak transcription	Fetal Muscle Trunk	muscle
29	chr3:17411600-17443400	Weak transcription	Rectal Smooth Muscle	rectum
30	chr3:17411800-17449200	Weak transcription	Stomach Smooth Muscle	stomach
31	chr3:17412200-17432200	Weak transcription	NH-A	brain
32	chr3:17412200-17437800	Weak transcription	GM12878-XiMat	blood
33	chr3:17412800-17450600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr3:17413000-17422000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:17413000-17443400	Weak transcription	Duodenum Mucosa	Duodenum
36	chr3:17413400-17445000	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr3:17413400-17453400	Weak transcription	Psoas Muscle	Psoas
38	chr3:17413600-17430200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr3:17413600-17430600	Weak transcription	Primary T cells from cord blood	blood
40	chr3:17413600-17430800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr3:17413600-17430800	Weak transcription	Left Ventricle	heart
42	chr3:17413600-17431000	Weak transcription	Placenta	Placenta
43	chr3:17413600-17432400	Weak transcription	Ovary	ovary
44	chr3:17413600-17435600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr3:17413600-17443400	Weak transcription	Fetal Lung	lung
46	chr3:17413600-17445400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr3:17413600-17447600	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr3:17413600-17449400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr3:17413800-17420400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:17413800-17426000	Weak transcription	Liver	Liver

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