Variant report

Variant	nsv519773
Chromosome Location	chr10:5904300-5905231
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:138)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:138 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:5904094-5905203	GM12878	blood:	n/a	n/a
2	ATF2	chr10:5904071-5905027	GM12878	blood:	n/a	n/a
3	BATF	chr10:5904143-5905100	GM12878	blood:	n/a	n/a
4	BATF	chr10:5904206-5904991	GM12878	blood:	n/a	n/a
5	BCL11A	chr10:5904162-5905104	GM12878	blood:	n/a	n/a
6	BCL11A	chr10:5904278-5904614	GM12878	blood:	n/a	n/a
7	BCL3	chr10:5904200-5904748	GM12878	blood:	n/a	n/a
8	BCLAF1	chr10:5904038-5904983	GM12878	blood:	n/a	n/a
9	BCLAF1	chr10:5904086-5905107	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:5904170-5904892	GM12878	blood:	n/a	n/a
11	CEBPB	chr10:5904286-5904770	GM12878	blood:	n/a	n/a
12	CEBPB	chr10:5904056-5904980	GM12878	blood:	n/a	n/a
13	CEBPB	chr10:5904144-5904329	HepG2	liver:	n/a	n/a
14	CHD1	chr10:5904267-5904867	GM12878	blood:	n/a	n/a
15	CHD2	chr10:5904177-5905077	GM12878	blood:	n/a	n/a
16	CREB1	chr10:5904117-5905044	GM12878	blood:	n/a	n/a
17	CREB1	chr10:5904075-5905144	GM12878	blood:	n/a	n/a
18	CTCF	chr10:5905040-5905190	HMF	breast:	n/a	n/a
19	CTCF	chr10:5905020-5905170	HEK293	kidney:	n/a	n/a
20	CTCF	chr10:5905100-5905250	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr10:5905040-5905190	AG04449	skin:	n/a	n/a
22	CTCF	chr10:5905080-5905230	HFF	foreskin:	n/a	n/a
23	CTCF	chr10:5905132-5905212	HepG2	liver:	n/a	n/a
24	CTCF	chr10:5905100-5905250	GM12873	blood:	n/a	n/a
25	CTCF	chr10:5905100-5905250	GM12871	blood:	n/a	n/a
26	CTCF	chr10:5904483-5905254	GM12878	blood:	n/a	n/a
27	CTCF	chr10:5905020-5905170	HepG2	liver:	n/a	n/a
28	CTCF	chr10:5905116-5905183	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr10:5905160-5905310	HCT-116	colon:	n/a	n/a
30	CTCF	chr10:5905100-5905250	GM12868	blood:	n/a	n/a
31	CTCF	chr10:5905100-5905250	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr10:5905020-5905170	RPTEC	kidney:	n/a	n/a
33	CTCF	chr10:5905100-5905250	A549	lung:	n/a	n/a
34	CTCF	chr10:5905080-5905230	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr10:5905160-5905310	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr10:5905060-5905210	HVMF	connective:	n/a	n/a
37	CUX1	chr10:5904260-5904824	GM12878	blood:	n/a	n/a
38	EBF1	chr10:5904081-5905014	GM12878	blood:	n/a	n/a
39	EBF1	chr10:5904140-5904870	GM12878	blood:	n/a	n/a
40	EBF1	chr10:5904188-5905055	GM12878	blood:	n/a	n/a
41	EGR1	chr10:5904399-5904649	GM12878	blood:	n/a	n/a
42	EGR1	chr10:5904393-5904659	GM12878	blood:	n/a	n/a
43	ELF1	chr10:5904152-5904932	GM12878	blood:	n/a	n/a
44	ELK1	chr10:5904248-5904512	GM12878	blood:	n/a	n/a
45	EP300	chr10:5904235-5904738	GM12878	blood:	n/a	n/a
46	EP300	chr10:5904186-5905099	GM12878	blood:	n/a	n/a
47	EP300	chr10:5904184-5905009	GM12878	blood:	n/a	n/a
48	ESRRA	chr10:5904023-5905341	GM12878	blood:	n/a	n/a
49	FOXA2	chr10:5904136-5904344	HepG2	liver:	n/a	n/a
50	FOXM1	chr10:5904117-5904966	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5904561-5904611	PrEC	prostate:	n/a
2	chr10:5904561-5904611	MCF-7	breast:	n/a
3	chr10:5904561-5904611	LNCaP	prostate:	n/a
4	chr10:5904561-5904611	HepG2	liver:	n/a
5	chr10:5904561-5904611	HCPEpiC	choroid plexus:	n/a
6	chr10:5904561-5904611	HCT-116	colon:	n/a
7	chr10:5904561-5904611	NH-A	brain:	n/a
8	chr10:5904561-5904611	HCM	heart:	n/a
9	chr10:5904561-5904611	RPTEC	kidney:	n/a
10	chr10:5904561-5904611	H1-hESC	embryonic stem cell:	embryo
11	chr10:5904561-5904611	ECC-1	luminal epithelium:	n/a
12	chr10:5904561-5904611	HPAEpiC	pulmonary alveolar:	n/a
13	chr10:5904561-5904611	NHDF-neo	bronchial:	n/a
14	chr10:5904561-5904611	HEEpiC	esophagus:	n/a
15	chr10:5904561-5904611	U87	brain:	n/a
16	chr10:5904561-5904611	BJ	skin:	n/a
17	chr10:5904561-5904611	NT2-D1	testis:	n/a
18	chr10:5904561-5904611	HUVEC	blood vessel:	n/a
19	chr10:5904561-5904611	T-47D	breast:	n/a
20	chr10:5904561-5904611	PANC-1	pancreas:	n/a
21	chr10:5904561-5904611	AG04449	skin:	fetal
22	chr10:5904561-5904611	HRCEpiC	kidney:	n/a
23	chr10:5904561-5904611	SK-N-MC	brain:	n/a
24	chr10:5904561-5904611	IMR90	lung:	fetal
25	chr10:5904561-5904611	AG04450	lung:	fetal
26	chr10:5904561-5904611	PFSK-1	brain:	n/a
27	chr10:5904561-5904611	AG10803	skin:	n/a
28	chr10:5904561-5904611	ProgFib	skin:	n/a
29	chr10:5904561-5904611	HIPEpiC	eye:	n/a
30	chr10:5904561-5904611	K562	blood:	n/a
31	chr10:5904561-5904611	HNPCEpiC	eye:	n/a
32	chr10:5904561-5904611	Caco-2	colon:	n/a
33	chr10:5904561-5904611	GM12891	blood:	n/a
34	chr10:5904561-5904611	NHBE	bronchial:	n/a
35	chr10:5904561-5904611	Hepatocyte	liver:	n/a
36	chr10:5904561-5904611	GM06990	blood:	n/a
37	chr10:5904561-5904611	Jurkat	blood:	n/a
38	chr10:5904561-5904611	HAEpiC	amniotic membrane:	n/a
39	chr10:5904561-5904611	ovcar-3	ovarian:	n/a
40	chr10:5904561-5904611	GM12892	blood:	n/a
41	chr10:5904561-5904611	SAEC	small airway:	n/a
42	chr10:5904561-5904611	MCF10A-Er-Src	breast:	n/a
43	chr10:5904561-5904611	AoSMC	blood vessel:	n/a
44	chr10:5904561-5904611	AG09309	skin:	n/a
45	chr10:5904561-5904611	GM19239	blood:	n/a
46	chr10:5904561-5904611	SKMC	muscle:	n/a
47	chr10:5904561-5904611	Hela-S3	cervix:	n/a
48	chr10:5904561-5904611	HMEC	breast:	n/a
49	chr10:5904561-5904611	SK-N-SH_RA	brain:	n/a
50	chr10:5904561-5904611	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:5853575..5857221-chr10:5900529..5905112,5	MCF-7	breast:
2	chr10:5904346..5907644-chr10:5928919..5931742,3	MCF-7	breast:
3	chr10:5903402..5905306-chr10:5930976..5933543,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GDI2-2	chr10:5904161-5904557	NONHSAT011187

No data

Variant related genes	Relation type
ENSG00000240180	TF binding region
ENSG00000240180	CpG island
ENSG00000134461	chromatin interactions
ENSG00000134452	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000272764	chromatin interactions

Extended variants
information (count: 40 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:40 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7913112	chr10:5904300-5904301	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187318065	chr10:5904301-5904302	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs565314162	chr10:5904323-5904324	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs145857114	chr10:5904348-5904349	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs76610235	chr10:5904371-5904372	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs560347702	chr10:5904423-5904424	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs527483004	chr10:5904437-5904438	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs557822825	chr10:5904455-5904456	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs548775578	chr10:5904513-5904514	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs138480783	chr10:5904536-5904537	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs77430848	chr10:5904549-5904550	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs549342597	chr10:5904562-5904563	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs79066356	chr10:5904622-5904623	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs141348199	chr10:5904648-5904649	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs61832916	chr10:5904661-5904662	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs192669088	chr10:5904677-5904678	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs150254423	chr10:5904692-5904693	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs554734886	chr10:5904713-5904714	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs576468829	chr10:5904752-5904753	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs7923781	chr10:5904760-5904761	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs76495255	chr10:5904772-5904773	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs577318443	chr10:5904810-5904811	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs528264245	chr10:5904817-5904818	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs545275544	chr10:5904868-5904869	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs2203197	chr10:5904918-5904919	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs527457391	chr10:5904948-5904949	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs74492186	chr10:5904974-5904975	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs183242629	chr10:5904975-5904976	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs72774167	chr10:5905017-5905018	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs187562803	chr10:5905046-5905047	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs549503998	chr10:5905063-5905064	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs570871612	chr10:5905087-5905088	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs374489130	chr10:5905098-5905099	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs113330159	chr10:5905125-5905126	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs377395042	chr10:5905133-5905134	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs566379410	chr10:5905152-5905153	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs79536520	chr10:5905167-5905168	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs138432392	chr10:5905203-5905204	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs570203684	chr10:5905224-5905225	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs980230	chr10:5905231-5905232	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5888800-5904400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:5894600-5908600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr10:5894600-5908600	Weak transcription	K562	blood
4	chr10:5894600-5916800	Weak transcription	Spleen	Spleen
5	chr10:5896200-5912200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr10:5896400-5918200	Weak transcription	Fetal Lung	lung
7	chr10:5899800-5905000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:5900000-5916600	Weak transcription	Pancreas	Pancrea
9	chr10:5900400-5916200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr10:5900600-5916200	Weak transcription	Stomach Smooth Muscle	stomach
11	chr10:5900800-5910600	Weak transcription	Brain Germinal Matrix	brain
12	chr10:5901000-5916600	Weak transcription	Gastric	stomach
13	chr10:5901200-5918200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr10:5901400-5905000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr10:5901400-5915200	Weak transcription	Brain Hippocampus Middle	brain
16	chr10:5901600-5912600	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr10:5901600-5915600	Weak transcription	Brain Anterior Caudate	brain
18	chr10:5901800-5910800	Weak transcription	Fetal Brain Female	brain
19	chr10:5902000-5904800	Enhancers	Placenta	Placenta
20	chr10:5902200-5904600	Enhancers	NHDF-Ad	bronchial
21	chr10:5902200-5905000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr10:5902200-5912600	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr10:5902400-5904400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr10:5902400-5905000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr10:5902400-5908600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr10:5902400-5918200	Weak transcription	Primary T cells from cord blood	blood
27	chr10:5902600-5904600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr10:5902600-5910200	Weak transcription	Fetal Muscle Leg	muscle
29	chr10:5902800-5916200	Weak transcription	Fetal Intestine Large	intestine
30	chr10:5902800-5916600	Weak transcription	Brain Substantia Nigra	brain
31	chr10:5902800-5918000	Weak transcription	Lung	lung
32	chr10:5903000-5904400	Enhancers	HSMM	muscle
33	chr10:5903000-5904600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr10:5903000-5905200	Enhancers	HepG2	liver
35	chr10:5903000-5912400	Weak transcription	Fetal Heart	heart
36	chr10:5903000-5915400	Weak transcription	Duodenum Mucosa	Duodenum
37	chr10:5903200-5904400	Enhancers	HUVEC	blood vessel
38	chr10:5903400-5911000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr10:5903400-5918200	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr10:5903400-5925000	Weak transcription	Fetal Kidney	kidney
41	chr10:5903600-5904400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr10:5903600-5904600	Enhancers	Osteobl	bone
43	chr10:5903600-5904800	Enhancers	Hela-S3	cervix
44	chr10:5903600-5904800	Enhancers	NHLF	lung
45	chr10:5903600-5916600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr10:5903800-5904400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr10:5903800-5904600	Enhancers	NH-A	brain
48	chr10:5903800-5905400	Enhancers	Primary B cells from peripheral blood	blood
49	chr10:5903800-5907200	Strong transcription	Fetal Stomach	stomach
50	chr10:5903800-5913600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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