Variant report

Variant	nsv895382
Chromosome Location	chr10:51330433-51515534
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1130)
CpG islands
(count:1101)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:51510620-51510822	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:51498525-51498807	HepG2	liver:	n/a	n/a
3	ATF1	chr10:51493021-51493256	K562	blood:	n/a	n/a
4	BACH1	chr10:51515004-51515258	K562	blood:	n/a	n/a
5	BACH1	chr10:51488208-51489253	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:51488154-51489051	K562	blood:	n/a	n/a
7	BACH1	chr10:51497179-51497372	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr10:51370987-51371657	GM12878	blood:	n/a	n/a
9	BATF	chr10:51377468-51377823	GM12878	blood:	n/a	n/a
10	BATF	chr10:51377417-51377859	GM12878	blood:	n/a	n/a
11	BCL11A	chr10:51377445-51377837	GM12878	blood:	n/a	n/a
12	BCL11A	chr10:51371338-51371706	GM12878	blood:	n/a	n/a
13	BCL11A	chr10:51371149-51371328	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:51502600-51502958	GM12878	blood:	n/a	n/a
15	BCL11A	chr10:51477990-51478142	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:51514477-51514595	K562	blood:	n/a	n/a
17	BHLHE40	chr10:51503123-51503576	K562	blood:	n/a	n/a
18	BHLHE40	chr10:51510685-51511217	HepG2	liver:	n/a	n/a
19	BHLHE40	chr10:51515168-51515875	K562	blood:	n/a	n/a
20	BHLHE40	chr10:51503018-51503229	GM12878	blood:	n/a	n/a
21	BHLHE40	chr10:51501363-51501407	K562	blood:	n/a	n/a
22	BHLHE40	chr10:51488172-51489419	K562	blood:	n/a	chr10:51489310-51489326
23	BHLHE40	chr10:51500736-51501099	K562	blood:	n/a	n/a
24	BHLHE40	chr10:51370779-51370981	HepG2	liver:	n/a	n/a
25	BRCA1	chr10:51496898-51497079	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr10:51503598-51503642	GM12878	blood:	n/a	n/a
27	BRCA1	chr10:51500821-51501021	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr10:51371133-51371579	K562	blood:	n/a	n/a
29	CBX3	chr10:51488737-51489298	K562	blood:	n/a	n/a
30	CBX3	chr10:51370429-51371746	K562	blood:	n/a	n/a
31	CCNT2	chr10:51488785-51489504	K562	blood:	n/a	n/a
32	CEBPB	chr10:51504781-51505050	K562	blood:	n/a	chr10:51504888-51504899
33	CEBPB	chr10:51495783-51495916	HepG2	liver:	n/a	chr10:51495870-51495881
34	CEBPB	chr10:51495788-51495959	ECC-1	luminal epithelium:	n/a	chr10:51495870-51495881
35	CEBPB	chr10:51495776-51496002	H1-hESC	embryonic stem cell:	n/a	chr10:51495870-51495881
36	CEBPB	chr10:51500891-51500985	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr10:51504726-51504995	IMR90	lung:	n/a	chr10:51504888-51504899
38	CEBPB	chr10:51500840-51501123	HepG2	liver:	n/a	n/a
39	CEBPB	chr10:51504729-51505034	HepG2	liver:	n/a	chr10:51504888-51504899
40	CEBPB	chr10:51495750-51495957	MCF-7	breast:	n/a	chr10:51495870-51495881
41	CEBPB	chr10:51397664-51397920	K562	blood:	n/a	n/a
42	CEBPB	chr10:51495736-51495938	HepG2	liver:	n/a	chr10:51495870-51495881
43	CEBPB	chr10:51495708-51496045	IMR90	lung:	n/a	chr10:51495870-51495881
44	CEBPB	chr10:51362034-51362409	IMR90	lung:	n/a	n/a
45	CEBPB	chr10:51495703-51496065	HepG2	liver:	n/a	chr10:51495870-51495881
46	CEBPB	chr10:51362046-51362409	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr10:51500916-51501060	K562	blood:	n/a	n/a
48	CEBPB	chr10:51495728-51496020	Hela-S3	cervix:	n/a	chr10:51495870-51495881
49	CEBPD	chr10:51371138-51371633	K562	blood:	n/a	n/a
50	CHD2	chr10:51503127-51503253	GM12878	blood:	n/a	n/a

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:51491984-51492034	HCF	heart:	n/a
2	chr10:51487759-51487809	LNCaP	prostate:	n/a
3	chr10:51463156-51463206	ovcar-3	ovarian:	n/a
4	chr10:51491984-51492034	HCF	heart:	n/a
5	chr10:51487759-51487809	LNCaP	prostate:	n/a
6	chr10:51463156-51463206	ovcar-3	ovarian:	n/a
7	chr10:51371707-51371757	ECC-1	luminal epithelium:	n/a
8	chr10:51371707-51371757	ovcar-3	ovarian:	n/a
9	chr10:51361773-51361823	HCT-116	colon:	n/a
10	chr10:51463156-51463206	HNPCEpiC	eye:	n/a
11	chr10:51489223-51489273	K562	blood:	n/a
12	chr10:51461855-51461905	AG04450	lung:	fetal
13	chr10:51374253-51374303	HEK293	kidney:	embryo
14	chr10:51487635-51487685	RPTEC	kidney:	n/a
15	chr10:51371691-51371741	SKMC	muscle:	n/a
16	chr10:51487759-51487809	AG04450	lung:	fetal
17	chr10:51361773-51361823	H1-hESC	embryonic stem cell:	embryo
18	chr10:51371709-51371759	NHBE	bronchial:	n/a
19	chr10:51491984-51492034	ProgFib	skin:	n/a
20	chr10:51463156-51463206	SK-N-SH	brain:	n/a
21	chr10:51487635-51487685	HEEpiC	esophagus:	n/a
22	chr10:51465444-51465494	MCF10A-Er-Src	breast:	n/a
23	chr10:51461855-51461905	CMK	blood:	n/a
24	chr10:51489643-51489693	ovcar-3	ovarian:	n/a
25	chr10:51465444-51465494	NB4	blood:	n/a
26	chr10:51491984-51492034	NH-A	brain:	n/a
27	chr10:51489510-51489560	HRPEpiC	eye:	n/a
28	chr10:51374253-51374303	T-47D	breast:	n/a
29	chr10:51371709-51371759	AG09319	gingival:	n/a
30	chr10:51361773-51361823	NHDF-neo	bronchial:	n/a
31	chr10:51489980-51490030	CMK	blood:	n/a
32	chr10:51491984-51492034	HL-60	blood:	n/a
33	chr10:51374253-51374303	SK-N-SH	brain:	n/a
34	chr10:51371709-51371759	AG04450	lung:	fetal
35	chr10:51489643-51489693	T-47D	breast:	n/a
36	chr10:51489643-51489693	Hela-S3	cervix:	n/a
37	chr10:51487635-51487685	HRCEpiC	kidney:	n/a
38	chr10:51361773-51361823	U87	brain:	n/a
39	chr10:51371707-51371757	SAEC	small airway:	n/a
40	chr10:51489643-51489693	HCT-116	colon:	n/a
41	chr10:51461855-51461905	AoSMC	blood vessel:	n/a
42	chr10:51463156-51463206	SKMC	muscle:	n/a
43	chr10:51371707-51371757	HIPEpiC	eye:	n/a
44	chr10:51371707-51371757	PFSK-1	brain:	n/a
45	chr10:51489980-51490030	HUVEC	blood vessel:	n/a
46	chr10:51371709-51371759	ovcar-3	ovarian:	n/a
47	chr10:51488973-51489023	NH-A	brain:	n/a
48	chr10:51488973-51489023	HAEpiC	amniotic membrane:	n/a
49	chr10:51461855-51461905	ovcar-3	ovarian:	n/a
50	chr10:51468217-51468267	CMK	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:47654251..47654891-chr10:51488416..51489496,4	Hela-S3	cervix:
2	chr10:47654306..47654893-chr10:51488919..51489481,3	MCF-7	breast:
3	chr10:47653734..47654656-chr10:51488800..51489544,4	MCF-7	breast:
4	chr10:51507609..51510007-chr10:51564889..51566530,2	K562	blood:
5	chr10:51498114..51501016-chr10:51502450..51504451,2	MCF-7	breast:
6	chr10:51497870..51501630-chr10:51543327..51546015,3	MCF-7	breast:
7	chr10:51487738..51490469-chr10:51490768..51492273,2	MCF-7	breast:
8	chr10:47654274..47658037-chr10:51487059..51489810,4	K562	blood:
9	chr10:47652879..47654869-chr10:51487976..51491279,3	MCF-7	breast:
10	chr10:47637552..47640564-chr10:51501175..51503678,3	MCF-7	breast:
11	chr10:51489258..51491268-chr10:51531426..51533100,2	MCF-7	breast:
12	chr10:47653740..47654385-chr10:51488816..51489933,3	MCF-7	breast:
13	chr10:47652235..47655869-chr10:51487775..51491801,8	MCF-7	breast:
14	chr10:51488667..51489638-chr19:9250701..9251449,2	NB4	blood:
15	chr10:51498114..51501016-chr10:51502450..51504451,2	MCF-7	breast:
16	chr10:51487738..51490469-chr10:51490768..51492273,2	MCF-7	breast:
17	chr10:47654140..47654870-chr10:51488638..51489755,11	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MSMB-2	chr10:51383526-51383726	NONHSAT013336
2	lnc-TIMM23B-2	chr10:51339438-51339770	NONHSAT013334

No data

Variant related genes	Relation type
AGAP8	TF binding region
TIMM23B	TF binding region
ENSG00000225784	TF binding region
AGAP7	TF binding region
ENSG00000244393	TF binding region
ENSG00000236787	TF binding region
ENSG00000223182	TF binding region
AGAP8	CpG island
TIMM23B	CpG island
ENSG00000225784	CpG island
AGAP7	CpG island
ENSG00000244393	CpG island
ENSG00000236787	CpG island
ENSG00000223182	CpG island
ENSG00000130803	chromatin interactions
ENSG00000259942	chromatin interactions
ENSG00000138293	chromatin interactions
ENSG00000198250	chromatin interactions
ENSG00000228326	chromatin interactions

Extended variants
information (count: 1949 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1949 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550614919	chr10:51358452-51358453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs111823739	chr10:51358555-51358556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs56289921	chr10:51358601-51358602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569103446	chr10:51358638-51358639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536092271	chr10:51358639-51358640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548126700	chr10:51359171-51359172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548395610	chr10:51359176-51359177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373340095	chr10:51359216-51359217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377245965	chr10:51359311-51359312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61848771	chr10:51359340-51359341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376287105	chr10:51359373-51359374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143350914	chr10:51359383-51359384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143627129	chr10:51359384-51359385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558648447	chr10:51359426-51359427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201247590	chr10:51359714-51359715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202215402	chr10:51359741-51359742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200349506	chr10:51359743-51359744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557396513	chr10:51360755-51360756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376905389	chr10:51360808-51360809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575876170	chr10:51360824-51360825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201406454	chr10:51360976-51360977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201867905	chr10:51361021-51361022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs61848781	chr10:51361088-51361089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561905395	chr10:51361292-51361293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530742959	chr10:51361320-51361321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs202084750	chr10:51361729-51361730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183831125	chr10:51361732-51361733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570728496	chr10:51361762-51361763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200401326	chr10:51361785-51361786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201204635	chr10:51361850-51361851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565003848	chr10:51361900-51361901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs199667579	chr10:51361901-51361902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550938235	chr10:51362025-51362026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562682761	chr10:51362032-51362033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200702902	chr10:51362041-51362042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529999035	chr10:51362043-51362044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548458672	chr10:51362141-51362142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566684818	chr10:51362163-51362164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533942907	chr10:51362164-51362165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552325536	chr10:51362221-51362222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570507451	chr10:51362234-51362235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201555796	chr10:51362316-51362317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556112290	chr10:51362357-51362358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199679342	chr10:51362425-51362426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372593743	chr10:51362454-51362455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370982564	chr10:51362455-51362456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575893672	chr10:51362487-51362488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201746276	chr10:51362547-51362548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536952265	chr10:51362650-51362651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200552107	chr10:51362862-51362863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
Autism	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	21935476	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:907 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:51358400-51370800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr10:51370800-51371200	Active TSS	H1 Cell Line	embryonic stem cell
3	chr10:51370800-51371200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr10:51370800-51371200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:51370800-51371200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr10:51370800-51371200	Active TSS	H9 Cell Line	embryonic stem cell
7	chr10:51370800-51371200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr10:51370800-51371200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr10:51370800-51371200	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr10:51370800-51371200	Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr10:51370800-51371200	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr10:51370800-51371200	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr10:51370800-51371200	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr10:51370800-51371200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr10:51370800-51371200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr10:51370800-51371200	Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr10:51370800-51371200	Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr10:51370800-51371200	Active TSS	Muscle Satellite Cultured Cells	--
19	chr10:51370800-51371200	Active TSS	Cortex derived primary cultured neurospheres	brain
20	chr10:51370800-51371200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr10:51370800-51371200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr10:51370800-51371200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr10:51370800-51371200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr10:51370800-51371200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
25	chr10:51370800-51371200	Active TSS	Brain Angular Gyrus	brain
26	chr10:51370800-51371200	Active TSS	Brain Anterior Caudate	brain
27	chr10:51370800-51371200	Active TSS	Brain Cingulate Gyrus	brain
28	chr10:51370800-51371200	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr10:51370800-51371200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr10:51370800-51371200	Active TSS	Duodenum Mucosa	Duodenum
31	chr10:51370800-51371200	Active TSS	Esophagus	oesophagus
32	chr10:51370800-51371200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
33	chr10:51370800-51371200	Active TSS	Fetal Brain Female	brain
34	chr10:51370800-51371200	Active TSS	Fetal Intestine Large	intestine
35	chr10:51370800-51371200	Active TSS	Fetal Intestine Small	intestine
36	chr10:51370800-51371200	Active TSS	Fetal Muscle Trunk	muscle
37	chr10:51370800-51371200	Active TSS	Fetal Stomach	stomach
38	chr10:51370800-51371200	Active TSS	Gastric	stomach
39	chr10:51370800-51371200	Active TSS	Pancreas	Pancrea
40	chr10:51370800-51371200	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr10:51370800-51371200	Active TSS	Right Atrium	heart
42	chr10:51370800-51371200	Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr10:51370800-51371200	Active TSS	Stomach Smooth Muscle	stomach
44	chr10:51370800-51371200	Active TSS	HMEC	breast
45	chr10:51370800-51371200	Active TSS	HSMM	muscle
46	chr10:51370800-51371200	Active TSS	HSMMtube	muscle
47	chr10:51370800-51371200	Active TSS	NHEK	skin
48	chr10:51370800-51371200	Active TSS	Osteobl	bone
49	chr10:51370800-51371800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr10:51370800-51371800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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