Variant report

Variant	nsv1033202
Chromosome Location	chr5:112891857-112945992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:112944089-112944147	K562	blood:	n/a	n/a
2	CEBPB	chr5:112943062-112943464	MCF-7	breast:	n/a	chr5:112943248-112943259
3	CEBPB	chr5:112943179-112943368	K562	blood:	n/a	chr5:112943248-112943259
4	CEBPB	chr5:112943159-112943418	Hela-S3	cervix:	n/a	chr5:112943248-112943259
5	CEBPB	chr5:112937565-112937748	A549	lung:	n/a	chr5:112937630-112937641
6	CEBPB	chr5:112910219-112910486	IMR90	lung:	n/a	n/a
7	CEBPB	chr5:112945293-112945296	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:112916537-112916820	K562	blood:	n/a	n/a
9	CEBPB	chr5:112943097-112943371	H1-hESC	embryonic stem cell:	n/a	chr5:112943248-112943259
10	CEBPB	chr5:112943068-112943444	HepG2	liver:	n/a	chr5:112943248-112943259
11	CEBPB	chr5:112937530-112937730	HepG2	liver:	n/a	chr5:112937630-112937641
12	CEBPB	chr5:112943067-112943431	A549	lung:	n/a	chr5:112943248-112943259
13	CEBPB	chr5:112943066-112943435	IMR90	lung:	n/a	chr5:112943248-112943259
14	CEBPB	chr5:112943067-112943440	K562	blood:	n/a	chr5:112943248-112943259
15	CEBPB	chr5:112943069-112943435	K562	blood:	n/a	chr5:112943248-112943259
16	CEBPB	chr5:112937613-112937698	H1-hESC	embryonic stem cell:	n/a	chr5:112937630-112937641
17	CTCF	chr5:112942380-112942530	NHEK	skin:	n/a	n/a
18	CTCF	chr5:112942020-112942170	AG04449	skin:	n/a	n/a
19	CTCF	chr5:112942340-112942490	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr5:112942360-112942510	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr5:112942340-112942490	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:112942360-112942510	HFF	foreskin:	n/a	n/a
23	CTCF	chr5:112942245-112942627	A549	lung:	n/a	n/a
24	CTCF	chr5:112942225-112942580	K562	blood:	n/a	n/a
25	CTCF	chr5:112942360-112942510	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr5:112897854-112897888	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr5:112942340-112942490	GM12864	blood:	n/a	n/a
28	CTCF	chr5:112942295-112942574	Medullo	brain:	n/a	n/a
29	CTCF	chr5:112942290-112942570	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr5:112942360-112942510	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr5:112929040-112929190	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:112942360-112942510	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr5:112942380-112942530	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr5:112942340-112942490	GM12873	blood:	n/a	n/a
35	CTCF	chr5:112941900-112942050	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr5:112942340-112942490	Caco-2	colon:	n/a	n/a
37	CTCF	chr5:112942309-112942565	HepG2	liver:	n/a	n/a
38	CTCF	chr5:112942380-112942530	BJ	skin:	n/a	n/a
39	CTCF	chr5:112942380-112942530	GM12867	blood:	n/a	n/a
40	CTCF	chr5:112942340-112942490	HMF	breast:	n/a	n/a
41	CTCF	chr5:112941962-112942699	HCT-116	colon:	n/a	n/a
42	CTCF	chr5:112942330-112942499	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr5:112941957-112942756	HCT-116	colon:	n/a	n/a
44	CTCF	chr5:112942380-112942530	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr5:112942400-112942550	WI-38	lung:	n/a	n/a
46	CTCF	chr5:112942380-112942530	GM12873	blood:	n/a	n/a
47	CTCF	chr5:112942260-112942410	HCT-116	colon:	n/a	n/a
48	CTCF	chr5:112942380-112942530	RPTEC	kidney:	n/a	n/a
49	CTCF	chr5:112942420-112942570	K562	blood:	n/a	n/a
50	CTCF	chr5:112942277-112942548	Fibrobl	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:112930120-112930170	NHBE	bronchial:	n/a
2	chr5:112930120-112930170	Caco-2	colon:	n/a
3	chr5:112930120-112930170	GM19239	blood:	n/a
4	chr5:112930120-112930170	RPTEC	kidney:	n/a
5	chr5:112930120-112930170	SK-N-MC	brain:	n/a
6	chr5:112930120-112930170	AG10803	skin:	n/a
7	chr5:112930120-112930170	HRPEpiC	eye:	n/a
8	chr5:112930120-112930170	AG09309	skin:	n/a
9	chr5:112930120-112930170	HEK293	kidney:	embryo
10	chr5:112930120-112930170	NH-A	brain:	n/a
11	chr5:112930120-112930170	GM12878	blood:	n/a
12	chr5:112930120-112930170	MCF10A-Er-Src	breast:	n/a
13	chr5:112930120-112930170	NB4	blood:	n/a
14	chr5:112930120-112930170	HEEpiC	esophagus:	n/a
15	chr5:112930120-112930170	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:112930120-112930170	HCM	heart:	n/a
17	chr5:112930120-112930170	AG04449	skin:	fetal
18	chr5:112930120-112930170	K562	blood:	n/a
19	chr5:112930120-112930170	NHDF-neo	bronchial:	n/a
20	chr5:112930120-112930170	PrEC	prostate:	n/a
21	chr5:112930120-112930170	HCF	heart:	n/a
22	chr5:112930120-112930170	NT2-D1	testis:	n/a
23	chr5:112930120-112930170	H1-hESC	embryonic stem cell:	embryo
24	chr5:112930120-112930170	HRE	kidney:	n/a
25	chr5:112930120-112930170	HL-60	blood:	n/a
26	chr5:112930120-112930170	HCT-116	colon:	n/a
27	chr5:112930120-112930170	AoSMC	blood vessel:	n/a
28	chr5:112930120-112930170	U87	brain:	n/a
29	chr5:112930120-112930170	HCPEpiC	choroid plexus:	n/a
30	chr5:112930120-112930170	HIPEpiC	eye:	n/a
31	chr5:112930120-112930170	ECC-1	luminal epithelium:	n/a
32	chr5:112930120-112930170	HNPCEpiC	eye:	n/a
33	chr5:112930120-112930170	AG04450	lung:	fetal
34	chr5:112930120-112930170	AG09319	gingival:	n/a
35	chr5:112930120-112930170	ProgFib	skin:	n/a
36	chr5:112930120-112930170	HepG2	liver:	n/a
37	chr5:112930120-112930170	A549	lung:	n/a
38	chr5:112930120-112930170	SAEC	small airway:	n/a
39	chr5:112930120-112930170	LNCaP	prostate:	n/a
40	chr5:112930120-112930170	HAEpiC	amniotic membrane:	n/a
41	chr5:112930120-112930170	IMR90	lung:	fetal
42	chr5:112930120-112930170	CMK	blood:	n/a
43	chr5:112930120-112930170	SKMC	muscle:	n/a
44	chr5:112930120-112930170	GM06990	blood:	n/a
45	chr5:112930120-112930170	PANC-1	pancreas:	n/a
46	chr5:112930120-112930170	HRCEpiC	kidney:	n/a
47	chr5:112930120-112930170	HUVEC	blood vessel:	n/a
48	chr5:112930120-112930170	BJ	skin:	n/a
49	chr5:112930120-112930170	GM12891	blood:	n/a
50	chr5:112930120-112930170	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:112926184..112928429-chr5:112930573..112932971,3	K562	blood:
2	chr5:112672794..112674511-chr5:112933592..112935108,2	MCF-7	breast:
3	chr5:112712448..112713203-chr5:112941932..112942910,3	K562	blood:
4	chr5:112923262..112928429-chr5:112929075..112932971,5	K562	blood:
5	chr5:112910971..112913788-chr5:112914677..112918901,4	K562	blood:
6	chr5:112883582..112886447-chr5:112891151..112893823,3	MCF-7	breast:
7	chr5:112919623..112922323-chr5:112924895..112926616,2	MCF-7	breast:
8	chr5:112850115..112851621-chr5:112917619..112919519,2	K562	blood:
9	chr5:112917130..112919077-chr5:112922484..112924889,2	K562	blood:
10	chr5:112919623..112922323-chr5:112924895..112926616,2	MCF-7	breast:
11	chr5:112672541..112673176-chr5:112942036..112942852,2	K562	blood:
12	chr5:112911409..112913819-chr5:112914953..112918122,3	K562	blood:
13	chr5:112917130..112919077-chr5:112922484..112924889,2	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	YTHDC2	hsa-miR-30c-5p	chr5:112929242-112929264
2	YTHDC2	hsa-miR-96-5p	chr5:112930241-112930263
3	YTHDC2	hsa-miR-30c-5p	chr5:112930813-112930835

Variant related genes	Relation type
YTHDC2	TF binding region
YTHDC2	CpG island
ENSG00000047188	chromatin interactions

Extended variants
information (count: 2329 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2329 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541645022	chr5:112891881-112891882	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370092984	chr5:112891887-112891888	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540791308	chr5:112891914-112891915	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35052193	chr5:112891915-112891916	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188805961	chr5:112891927-112891928	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546181957	chr5:112891975-112891976	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2162842	chr5:112892000-112892001	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs543053097	chr5:112892027-112892028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115738497	chr5:112892061-112892062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs67723806	chr5:112892124-112892125	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs200419259	chr5:112892142-112892143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147928136	chr5:112892163-112892164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571882379	chr5:112892189-112892190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34554590	chr5:112892277-112892278	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs112315663	chr5:112892290-112892291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75880766	chr5:112892320-112892321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141910023	chr5:112892352-112892353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377389768	chr5:112892353-112892354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565810041	chr5:112892365-112892366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181526903	chr5:112892410-112892411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77651825	chr5:112892412-112892413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528487541	chr5:112892414-112892415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375291397	chr5:112892415-112892416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554593231	chr5:112892432-112892433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569562619	chr5:112892441-112892442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537019160	chr5:112892466-112892467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186176908	chr5:112892500-112892501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150477844	chr5:112892509-112892510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75636012	chr5:112892510-112892511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111801112	chr5:112892517-112892518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114380680	chr5:112892534-112892535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567744309	chr5:112892558-112892559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538477162	chr5:112892559-112892560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149037541	chr5:112892610-112892611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542763354	chr5:112892619-112892620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111891792	chr5:112892645-112892646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531630155	chr5:112892681-112892682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113797703	chr5:112892682-112892683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565612285	chr5:112892711-112892712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556734198	chr5:112892745-112892746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs578074366	chr5:112892749-112892750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77435604	chr5:112892760-112892761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374483432	chr5:112892763-112892764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548058725	chr5:112892799-112892800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143013060	chr5:112892800-112892801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367755708	chr5:112892833-112892834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10478127	chr5:112892836-112892837	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs138596717	chr5:112892845-112892846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571753577	chr5:112892887-112892888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536678927	chr5:112892893-112892894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	22495309	CNVD

Chromatin state (count:1356 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112850400-112904000	Weak transcription	Psoas Muscle	Psoas
2	chr5:112850600-112908400	Weak transcription	Colonic Mucosa	Colon
3	chr5:112851600-112893200	Weak transcription	Fetal Brain Male	brain
4	chr5:112851600-112902800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr5:112867000-112910000	Weak transcription	Right Ventricle	heart
6	chr5:112867200-112903400	Weak transcription	Pancreas	Pancrea
7	chr5:112867200-112904000	Weak transcription	Lung	lung
8	chr5:112867200-112904200	Weak transcription	Aorta	Aorta
9	chr5:112867200-112909800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr5:112867200-112909800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr5:112867200-112910000	Weak transcription	Esophagus	oesophagus
12	chr5:112867400-112926000	Weak transcription	Small Intestine	intestine
13	chr5:112867400-112933000	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr5:112868000-112893400	Strong transcription	Dnd41	blood
15	chr5:112868400-112893600	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr5:112868600-112911400	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr5:112869200-112910000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr5:112870200-112930800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr5:112872000-112904000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:112872000-112915000	Weak transcription	Hela-S3	cervix
21	chr5:112873000-112894000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:112873000-112900600	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr5:112873400-112908800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr5:112874000-112909600	Weak transcription	Spleen	Spleen
25	chr5:112874400-112902600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:112876000-112918800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr5:112877200-112905800	Weak transcription	Fetal Stomach	stomach
28	chr5:112877400-112892000	Weak transcription	Brain Germinal Matrix	brain
29	chr5:112878200-112894000	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr5:112879600-112895200	Weak transcription	Left Ventricle	heart
31	chr5:112879600-112902800	Weak transcription	Thymus	Thymus
32	chr5:112879600-112904200	Weak transcription	Gastric	stomach
33	chr5:112881800-112906400	Weak transcription	Fetal Intestine Small	intestine
34	chr5:112882000-112893400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr5:112882600-112904000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr5:112882800-112909600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr5:112883000-112899600	Weak transcription	Brain Angular Gyrus	brain
38	chr5:112883000-112903200	Weak transcription	Rectal Smooth Muscle	rectum
39	chr5:112883200-112895200	Weak transcription	NHEK	skin
40	chr5:112883200-112896400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr5:112883400-112895400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:112883800-112893200	Strong transcription	Adipose Nuclei	Adipose
43	chr5:112883800-112907400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:112884200-112905200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr5:112884200-112905600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr5:112884200-112908000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:112884800-112893400	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr5:112884800-112896800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:112885400-112895000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr5:112885400-112897800	Weak transcription	Sigmoid Colon	Sigmoid Colon

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