Variant report

Variant	esv1844388
Chromosome Location	chr10:51371074-51521245
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1068)
CpG islands
(count:1039)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1068 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:51519621-51519799	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:51498525-51498807	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:51510620-51510822	HepG2	liver:	n/a	n/a
4	ATF1	chr10:51493021-51493256	K562	blood:	n/a	n/a
5	ATF1	chr10:51517350-51518597	K562	blood:	n/a	n/a
6	BACH1	chr10:51497179-51497372	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:51515004-51515258	K562	blood:	n/a	n/a
8	BACH1	chr10:51488208-51489253	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:51488154-51489051	K562	blood:	n/a	n/a
10	BATF	chr10:51377468-51377823	GM12878	blood:	n/a	n/a
11	BATF	chr10:51370987-51371657	GM12878	blood:	n/a	n/a
12	BATF	chr10:51377417-51377859	GM12878	blood:	n/a	n/a
13	BCL11A	chr10:51502600-51502958	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:51371338-51371706	GM12878	blood:	n/a	n/a
15	BCL11A	chr10:51371149-51371328	GM12878	blood:	n/a	n/a
16	BCL11A	chr10:51477990-51478142	GM12878	blood:	n/a	n/a
17	BCL11A	chr10:51377445-51377837	GM12878	blood:	n/a	n/a
18	BHLHE40	chr10:51503123-51503576	K562	blood:	n/a	n/a
19	BHLHE40	chr10:51500736-51501099	K562	blood:	n/a	n/a
20	BHLHE40	chr10:51501363-51501407	K562	blood:	n/a	n/a
21	BHLHE40	chr10:51510685-51511217	HepG2	liver:	n/a	n/a
22	BHLHE40	chr10:51503018-51503229	GM12878	blood:	n/a	n/a
23	BHLHE40	chr10:51515168-51515875	K562	blood:	n/a	n/a
24	BHLHE40	chr10:51488172-51489419	K562	blood:	n/a	chr10:51489310-51489326
25	BHLHE40	chr10:51514477-51514595	K562	blood:	n/a	n/a
26	BRCA1	chr10:51496898-51497079	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr10:51503598-51503642	GM12878	blood:	n/a	n/a
28	BRCA1	chr10:51500821-51501021	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr10:51488737-51489298	K562	blood:	n/a	n/a
30	CBX3	chr10:51371133-51371579	K562	blood:	n/a	n/a
31	CBX3	chr10:51370429-51371746	K562	blood:	n/a	n/a
32	CCNT2	chr10:51488785-51489504	K562	blood:	n/a	n/a
33	CCNT2	chr10:51518348-51518584	K562	blood:	n/a	n/a
34	CEBPB	chr10:51495736-51495938	HepG2	liver:	n/a	chr10:51495870-51495881
35	CEBPB	chr10:51518182-51518550	K562	blood:	n/a	n/a
36	CEBPB	chr10:51495750-51495957	MCF-7	breast:	n/a	chr10:51495870-51495881
37	CEBPB	chr10:51397664-51397920	K562	blood:	n/a	n/a
38	CEBPB	chr10:51518156-51518550	A549	lung:	n/a	n/a
39	CEBPB	chr10:51500840-51501123	HepG2	liver:	n/a	n/a
40	CEBPB	chr10:51518199-51518577	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr10:51495788-51495959	ECC-1	luminal epithelium:	n/a	chr10:51495870-51495881
42	CEBPB	chr10:51495776-51496002	H1-hESC	embryonic stem cell:	n/a	chr10:51495870-51495881
43	CEBPB	chr10:51495783-51495916	HepG2	liver:	n/a	chr10:51495870-51495881
44	CEBPB	chr10:51518227-51518564	IMR90	lung:	n/a	n/a
45	CEBPB	chr10:51500891-51500985	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr10:51495708-51496045	IMR90	lung:	n/a	chr10:51495870-51495881
47	CEBPB	chr10:51504781-51505050	K562	blood:	n/a	chr10:51504888-51504899
48	CEBPB	chr10:51518221-51518550	HepG2	liver:	n/a	n/a
49	CEBPB	chr10:51495703-51496065	HepG2	liver:	n/a	chr10:51495870-51495881
50	CEBPB	chr10:51495728-51496020	Hela-S3	cervix:	n/a	chr10:51495870-51495881

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:51489223-51489273	AG04450	lung:	fetal
2	chr10:51491984-51492034	K562	blood:	n/a
3	chr10:51489223-51489273	AG04450	lung:	fetal
4	chr10:51491984-51492034	K562	blood:	n/a
5	chr10:51468217-51468267	HL-60	blood:	n/a
6	chr10:51488973-51489023	HAEpiC	amniotic membrane:	n/a
7	chr10:51374253-51374303	HRE	kidney:	n/a
8	chr10:51461855-51461905	HCT-116	colon:	n/a
9	chr10:51487759-51487809	HUVEC	blood vessel:	n/a
10	chr10:51465444-51465494	BJ	skin:	n/a
11	chr10:51487558-51487608	HEK293	kidney:	embryo
12	chr10:51463156-51463206	Hela-S3	cervix:	n/a
13	chr10:51489223-51489273	AG09309	skin:	n/a
14	chr10:51463156-51463206	HCT-116	colon:	n/a
15	chr10:51488973-51489023	Jurkat	blood:	n/a
16	chr10:51487558-51487608	U87	brain:	n/a
17	chr10:51371707-51371757	AG09309	skin:	n/a
18	chr10:51463156-51463206	U87	brain:	n/a
19	chr10:51465444-51465494	HEK293	kidney:	embryo
20	chr10:51491984-51492034	AG10803	skin:	n/a
21	chr10:51468217-51468267	HPAEpiC	pulmonary alveolar:	n/a
22	chr10:51371709-51371759	GM06990	blood:	n/a
23	chr10:51371691-51371741	LNCaP	prostate:	n/a
24	chr10:51465444-51465494	GM12878	blood:	n/a
25	chr10:51489980-51490030	NB4	blood:	n/a
26	chr10:51489643-51489693	NB4	blood:	n/a
27	chr10:51491984-51492034	HAEpiC	amniotic membrane:	n/a
28	chr10:51489980-51490030	MCF10A-Er-Src	breast:	n/a
29	chr10:51489980-51490030	AG04450	lung:	fetal
30	chr10:51487635-51487685	T-47D	breast:	n/a
31	chr10:51489643-51489693	ECC-1	luminal epithelium:	n/a
32	chr10:51487759-51487809	ECC-1	luminal epithelium:	n/a
33	chr10:51489643-51489693	Caco-2	colon:	n/a
34	chr10:51374253-51374303	HCPEpiC	choroid plexus:	n/a
35	chr10:51371691-51371741	PrEC	prostate:	n/a
36	chr10:51488973-51489023	IMR90	lung:	fetal
37	chr10:51487558-51487608	HRCEpiC	kidney:	n/a
38	chr10:51488973-51489023	BE2_C	brain:	n/a
39	chr10:51491984-51492034	HRPEpiC	eye:	n/a
40	chr10:51468217-51468267	HUVEC	blood vessel:	n/a
41	chr10:51489980-51490030	HL-60	blood:	n/a
42	chr10:51468217-51468267	AG09309	skin:	n/a
43	chr10:51487635-51487685	HEK293	kidney:	embryo
44	chr10:51487635-51487685	PrEC	prostate:	n/a
45	chr10:51468217-51468267	LNCaP	prostate:	n/a
46	chr10:51489510-51489560	AG09319	gingival:	n/a
47	chr10:51461855-51461905	ProgFib	skin:	n/a
48	chr10:51489510-51489560	GM12878	blood:	n/a
49	chr10:51488973-51489023	Hepatocyte	liver:	n/a
50	chr10:51374253-51374303	GM12892	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:47637552..47640564-chr10:51501175..51503678,3	MCF-7	breast:
2	chr10:47654306..47654893-chr10:51488919..51489481,3	MCF-7	breast:
3	chr10:51487738..51490469-chr10:51490768..51492273,2	MCF-7	breast:
4	chr10:51487738..51490469-chr10:51490768..51492273,2	MCF-7	breast:
5	chr10:47654274..47658037-chr10:51487059..51489810,4	K562	blood:
6	chr10:47652235..47655869-chr10:51487775..51491801,8	MCF-7	breast:
7	chr10:51488667..51489638-chr19:9250701..9251449,2	NB4	blood:
8	chr10:47653740..47654385-chr10:51488816..51489933,3	MCF-7	breast:
9	chr10:51497870..51501630-chr10:51543327..51546015,3	MCF-7	breast:
10	chr10:47652879..47654869-chr10:51487976..51491279,3	MCF-7	breast:
11	chr10:51519873..51522291-chr10:51523430..51526195,2	MCF-7	breast:
12	chr10:47654140..47654870-chr10:51488638..51489755,11	HCT-116	colon:
13	chr10:51498114..51501016-chr10:51502450..51504451,2	MCF-7	breast:
14	chr10:51498114..51501016-chr10:51502450..51504451,2	MCF-7	breast:
15	chr10:47653734..47654656-chr10:51488800..51489544,4	MCF-7	breast:
16	chr10:51507609..51510007-chr10:51564889..51566530,2	K562	blood:
17	chr10:47654251..47654891-chr10:51488416..51489496,4	Hela-S3	cervix:
18	chr10:51489258..51491268-chr10:51531426..51533100,2	MCF-7	breast:

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

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

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
ENSG00000223182	TF binding region
AGAP8	CpG island
TIMM23B	CpG island
ENSG00000225784	CpG island
AGAP7	CpG island
ENSG00000244393	CpG island
ENSG00000223182	CpG island
ENSG00000259942	chromatin interactions
ENSG00000228326	chromatin interactions
ENSG00000130803	chromatin interactions
ENSG00000138293	chromatin interactions
ENSG00000198250	chromatin interactions

Extended variants
information (count: 2021 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2021 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61848834	chr10:51371153-51371154	Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs201811271	chr10:51371256-51371257	Weak transcription Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs61848835	chr10:51371355-51371356	Weak transcription Active TSS	TF binding region	4 gene(s)	Overlapped CNVs	n/a
4	rs61848836	chr10:51371372-51371373	Weak transcription Active TSS	TF binding region	4 gene(s)	Overlapped CNVs	n/a
5	rs61848837	chr10:51371420-51371421	Weak transcription Active TSS	TF binding region	4 gene(s)	Overlapped CNVs	n/a
6	rs577319286	chr10:51371653-51371654	Weak transcription Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
7	rs544703271	chr10:51371694-51371695	Weak transcription Active TSS	TF binding region CpG island	3 gene(s)	Overlapped CNVs	n/a
8	rs556350367	chr10:51371742-51371743	Weak transcription Active TSS	TF binding region CpG island	3 gene(s)	Overlapped CNVs	n/a
9	rs367714213	chr10:51371951-51371952	Weak transcription Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
10	rs5000943	chr10:51372029-51372030	Weak transcription Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
11	rs5000942	chr10:51372058-51372059	Weak transcription Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
12	rs5000939	chr10:51372205-51372206	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
13	rs5000938	chr10:51372208-51372209	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
14	rs374661007	chr10:51372467-51372468	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
15	rs371954741	chr10:51372563-51372564	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
16	rs61848841	chr10:51372717-51372718	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
17	rs199791538	chr10:51373075-51373076	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
18	rs116868183	chr10:51373079-51373080	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
19	rs374469850	chr10:51373080-51373081	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
20	rs61848842	chr10:51373211-51373212	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
21	rs369718640	chr10:51373310-51373311	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
22	rs375634343	chr10:51373361-51373362	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
23	rs374092462	chr10:51373375-51373376	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
24	rs542223745	chr10:51373424-51373425	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
25	rs375126795	chr10:51373432-51373433	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
26	rs560474674	chr10:51373461-51373462	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
27	rs199564287	chr10:51373521-51373522	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
28	rs200844776	chr10:51373529-51373530	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
29	rs200580159	chr10:51373558-51373559	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
30	rs61848843	chr10:51373658-51373659	Weak transcription Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
31	rs61848844	chr10:51373660-51373661	Weak transcription Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
32	rs527573011	chr10:51373756-51373757	Weak transcription Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
33	rs546064990	chr10:51373762-51373763	Weak transcription Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
34	rs564305981	chr10:51373785-51373786	Weak transcription Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
35	rs531362571	chr10:51373787-51373788	Weak transcription Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
36	rs549863049	chr10:51373807-51373808	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
37	rs201170658	chr10:51373820-51373821	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
38	rs187475320	chr10:51373835-51373836	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
39	rs199640014	chr10:51374007-51374008	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
40	rs61848845	chr10:51374029-51374030	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
41	rs61848846	chr10:51374050-51374051	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
42	rs61849461	chr10:51374131-51374132	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
43	rs546972327	chr10:51374152-51374153	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
44	rs566871456	chr10:51374162-51374163	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
45	rs534226725	chr10:51374190-51374191	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
46	rs374661572	chr10:51374218-51374219	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
47	rs78115295	chr10:51374253-51374254	Weak transcription Enhancers	TF binding region CpG island	3 gene(s)	Overlapped CNVs	n/a
48	rs558945208	chr10:51374258-51374259	Weak transcription Enhancers	TF binding region CpG island	3 gene(s)	Overlapped CNVs	n/a
49	rs535522498	chr10:51374286-51374287	Weak transcription Enhancers	TF binding region CpG island	3 gene(s)	Overlapped CNVs	n/a
50	rs61849463	chr10:51374294-51374295	Weak transcription Enhancers	TF binding region CpG island	3 gene(s)	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:981 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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

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