Variant report

Variant	nsv590362
Chromosome Location	chr3:56594735-56661320
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:225)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:225 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:56650518-56650959	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:56650516-56650965	K562	blood:	n/a	n/a
3	BACH1	chr3:56645287-56645418	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr3:56625349-56625694	IMR90	lung:	n/a	n/a
5	CEBPB	chr3:56602814-56603020	HepG2	liver:	n/a	n/a
6	CTCF	chr3:56641131-56641251	Lung_OC	lung:	n/a	n/a
7	CTCF	chr3:56617432-56617474	GM10248	blood:	n/a	n/a
8	CTCF	chr3:56649436-56649475	ProgFib	skin:	n/a	n/a
9	CTCF	chr3:56617430-56617498	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr3:56605479-56605526	GM10248	blood:	n/a	n/a
11	CTCF	chr3:56602885-56602932	GM20000	blood:	n/a	n/a
12	CTCF	chr3:56617436-56617520	GM20000	blood:	n/a	n/a
13	CTCF	chr3:56600075-56600162	GM20000	blood:	n/a	n/a
14	CUX1	chr3:56650752-56650867	K562	blood:	n/a	n/a
15	E2F4	chr3:56650905-56651086	MCF10A-Er-Src	breast:	n/a	n/a
16	EP300	chr3:56650555-56650720	K562	blood:	n/a	n/a
17	FOS	chr3:56649395-56649664	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr3:56649450-56649587	MCF10A-Er-Src	breast:	n/a	n/a
19	FOXA1	chr3:56627522-56627727	T-47D	breast:	n/a	chr3:56627594-56627609
20	FOXA1	chr3:56607602-56607833	T-47D	breast:	n/a	n/a
21	FOXA2	chr3:56648935-56649091	HepG2	liver:	n/a	n/a
22	FOXA2	chr3:56615878-56616331	A549	lung:	n/a	n/a
23	GATA2	chr3:56607610-56607839	SH-SY5Y	brain:	n/a	n/a
24	GATA3	chr3:56607541-56607874	T-47D	breast:	n/a	n/a
25	GATA3	chr3:56658904-56659000	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr3:56607546-56607885	T-47D	breast:	n/a	n/a
27	GATA3	chr3:56607555-56607906	MCF-7	breast:	n/a	n/a
28	GATA3	chr3:56627441-56627733	T-47D	breast:	n/a	n/a
29	IRF1	chr3:56624954-56624962	K562	blood:	n/a	n/a
30	IRF1	chr3:56651392-56651440	K562	blood:	n/a	n/a
31	JUN	chr3:56624951-56625154	H1-hESC	embryonic stem cell:	n/a	n/a
32	JUN	chr3:56654256-56654535	K562	blood:	n/a	n/a
33	JUND	chr3:56608586-56608747	HepG2	liver:	n/a	n/a
34	KAT2A	chr3:56637051-56637417	GM12878	blood:	n/a	n/a
35	MAFF	chr3:56604285-56604493	HepG2	liver:	n/a	n/a
36	MAFF	chr3:56650515-56650889	K562	blood:	n/a	chr3:56650690-56650708
37	MAFF	chr3:56598963-56599087	HepG2	liver:	n/a	n/a
38	MAFF	chr3:56604291-56604461	K562	blood:	n/a	n/a
39	MAFF	chr3:56650512-56650906	HepG2	liver:	n/a	chr3:56650690-56650708
40	MAFK	chr3:56650512-56650947	Hela-S3	cervix:	n/a	chr3:56650692-56650707
41	MAFK	chr3:56604205-56604529	HepG2	liver:	n/a	chr3:56604361-56604376
42	MAFK	chr3:56650514-56650890	HepG2	liver:	n/a	chr3:56650692-56650707
43	MAFK	chr3:56650513-56650891	IMR90	lung:	n/a	chr3:56650692-56650707
44	MAFK	chr3:56650523-56650888	H1-hESC	embryonic stem cell:	n/a	chr3:56650692-56650707
45	MAFK	chr3:56645277-56645373	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAFK	chr3:56654465-56654697	HepG2	liver:	n/a	n/a
47	MAFK	chr3:56604211-56604490	IMR90	lung:	n/a	chr3:56604361-56604376
48	MAFK	chr3:56660693-56660862	IMR90	lung:	n/a	n/a
49	MAFK	chr3:56650509-56650888	K562	blood:	n/a	chr3:56650692-56650707
50	MAFK	chr3:56650525-56650954	HepG2	liver:	n/a	chr3:56650692-56650707

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:56619803..56621869-chr3:56626645..56628418,2	K562	blood:
2	chr3:56653784..56655338-chr3:56659121..56661544,2	K562	blood:
3	chr3:56590586..56593245-chr3:56606060..56608727,2	K562	blood:
4	chr3:56649555..56651399-chr3:56654571..56656999,2	MCF-7	breast:
5	chr3:56657076..56658980-chr3:56660607..56664141,3	K562	blood:
6	chr3:56650528..56653127-chr3:56654504..56656215,2	MCF-7	breast:
7	chr3:56654291..56656477-chr3:56715721..56718612,2	MCF-7	breast:
8	chr3:56655597..56657601-chr3:56661033..56663452,2	K562	blood:
9	chr3:56595109..56597404-chr3:56602239..56604027,2	K562	blood:
10	chr3:56590931..56593644-chr3:56601004..56602846,2	K562	blood:
11	chr3:56595109..56597404-chr3:56602239..56604027,2	K562	blood:
12	chr3:56647300..56648856-chr3:56648916..56651486,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPATA12-5	chr3:56626998-56627089	NONHSAT090054
2	lnc-SPATA12-5	chr3:56599162-56599205	NONHSAT090052
3	lnc-SPATA12-5	chr3:56594890-56595250	NONHSAT090051
4	lnc-SPATA12-5	chr3:56600979-56601081	NONHSAT090055
5	lnc-SPATA12-5	chr3:56600811-56601081	NONHSAT090054
6	lnc-SPATA12-5	chr3:56597544-56598153	NONHSAT090052
7	lnc-SPATA12-5	chr3:56606365-56606938	NONHSAT090053
8	lnc-SPATA12-5	chr3:56605209-56605330	NONHSAT090053
9	lnc-SPATA12-5	chr3:56600689-56600787	NONHSAT090053
10	lnc-SPATA12-5	chr3:56605209-56605407	NONHSAT090055
11	lnc-SPATA12-5	chr3:56600978-56601081	NONHSAT090053
12	lnc-SPATA12-5	chr3:56606365-56606456	NONHSAT090054
13	lnc-SPATA12-5	chr3:56605209-56605330	NONHSAT090054

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C3orf63	hsa-miR-34a-5p	chr3:56654302-56654325
2	C3orf63	hsa-miR-34a-5p	chr3:56654308-56654301

Variant related genes	Relation type
CCDC66	TF binding region
FAM208A	TF binding region
ENSG00000180376	chromatin interactions
ENSG00000163946	chromatin interactions

Extended variants
information (count: 2850 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2850 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9822876	chr3:56594735-56594736	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532650920	chr3:56594766-56594767	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546011331	chr3:56594778-56594779	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559686092	chr3:56594783-56594784	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190942198	chr3:56594839-56594840	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367986353	chr3:56594890-56594891	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs548563564	chr3:56594891-56594892	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs562002393	chr3:56595026-56595027	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs146669146	chr3:56595049-56595050	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs112001681	chr3:56595052-56595053	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs572085802	chr3:56595059-56595060	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs566110006	chr3:56595084-56595085	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs565523173	chr3:56595093-56595094	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs533434338	chr3:56595125-56595126	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs201503027	chr3:56595134-56595135	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs17825529	chr3:56595153-56595154	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs79017751	chr3:56595163-56595164	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs371600520	chr3:56595170-56595171	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs546344156	chr3:56595180-56595181	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs566584470	chr3:56595259-56595260	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs555547155	chr3:56595297-56595298	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs116527725	chr3:56595317-56595318	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs180887018	chr3:56595318-56595319	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs575602140	chr3:56595362-56595363	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs538191258	chr3:56595392-56595393	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs557963630	chr3:56595401-56595402	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs576336766	chr3:56595497-56595498	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs184903443	chr3:56595518-56595519	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs112157485	chr3:56595574-56595575	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs567022224	chr3:56595604-56595605	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs17216678	chr3:56595606-56595607	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs190152916	chr3:56595673-56595674	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs573295255	chr3:56595679-56595680	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs541846679	chr3:56595680-56595681	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs561792250	chr3:56595800-56595801	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs531086564	chr3:56595815-56595816	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs552536095	chr3:56595848-56595849	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550896273	chr3:56595852-56595853	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs564456000	chr3:56595903-56595904	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs143877291	chr3:56595909-56595910	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs371874736	chr3:56595922-56595923	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs146891954	chr3:56595928-56595929	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs535578269	chr3:56595954-56595955	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs577594734	chr3:56595956-56595957	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs182418949	chr3:56595957-56595958	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs538124906	chr3:56595995-56595996	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs75896189	chr3:56596037-56596038	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148980598	chr3:56596044-56596045	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577869389	chr3:56596053-56596054	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533705361	chr3:56596077-56596078	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Renal cell carcinoma	18765545	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:1991 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56591800-56596000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:56591800-56599800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:56592000-56615600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:56592200-56609400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr3:56592400-56594800	Weak transcription	Primary B cells from peripheral blood	blood
6	chr3:56592400-56594800	Weak transcription	HSMM	muscle
7	chr3:56592400-56596000	Weak transcription	Fetal Muscle Trunk	muscle
8	chr3:56592400-56596000	Weak transcription	Fetal Stomach	stomach
9	chr3:56592400-56596800	Weak transcription	Fetal Muscle Leg	muscle
10	chr3:56592400-56599800	Weak transcription	Fetal Lung	lung
11	chr3:56592400-56600000	Weak transcription	Ovary	ovary
12	chr3:56592400-56601200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr3:56592400-56601400	Weak transcription	Left Ventricle	heart
14	chr3:56592400-56601800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr3:56592400-56601800	Weak transcription	Lung	lung
16	chr3:56592400-56602000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr3:56592400-56602800	Weak transcription	Esophagus	oesophagus
18	chr3:56592400-56602800	Weak transcription	Gastric	stomach
19	chr3:56592400-56602800	Weak transcription	Spleen	Spleen
20	chr3:56592400-56603000	Weak transcription	Pancreas	Pancrea
21	chr3:56592400-56607400	Weak transcription	Psoas Muscle	Psoas
22	chr3:56592400-56615600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr3:56592400-56639800	Weak transcription	Right Ventricle	heart
24	chr3:56592400-56644800	Weak transcription	Small Intestine	intestine
25	chr3:56592600-56594800	Weak transcription	Liver	Liver
26	chr3:56592600-56594800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr3:56592600-56595600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr3:56592600-56595800	Weak transcription	Stomach Smooth Muscle	stomach
29	chr3:56592600-56596000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr3:56592600-56596000	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr3:56592600-56598600	Weak transcription	Brain Hippocampus Middle	brain
32	chr3:56592600-56598800	Weak transcription	Primary hematopoietic stem cells	blood
33	chr3:56592600-56599600	Weak transcription	Thymus	Thymus
34	chr3:56592600-56600000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr3:56592600-56600000	Weak transcription	Colonic Mucosa	Colon
36	chr3:56592600-56600200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr3:56592600-56600200	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr3:56592600-56600200	Weak transcription	NHLF	lung
39	chr3:56592600-56601000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr3:56592600-56601000	Weak transcription	HSMMtube	muscle
41	chr3:56592600-56601800	Weak transcription	Aorta	Aorta
42	chr3:56592600-56602200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr3:56592600-56602200	Weak transcription	Brain Germinal Matrix	brain
44	chr3:56592600-56602200	Weak transcription	Fetal Brain Male	brain
45	chr3:56592600-56603000	Weak transcription	Rectal Smooth Muscle	rectum
46	chr3:56592600-56603800	Weak transcription	Stomach Mucosa	stomach
47	chr3:56592800-56594800	Weak transcription	Primary B cells from cord blood	blood
48	chr3:56592800-56594800	Weak transcription	Adipose Nuclei	Adipose
49	chr3:56592800-56594800	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr3:56592800-56595200	Weak transcription	Muscle Satellite Cultured Cells	--

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