Variant report

Variant	esv2758215
Chromosome Location	chr10:42684893-42879686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1934)
CpG islands
(count:1403)
Chromatin interactive
region (count:13)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1934 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:42799540-42800192	HepG2	liver:	n/a	n/a
2	ATF1	chr10:42797113-42797490	K562	blood:	n/a	n/a
3	ATF1	chr10:42817203-42817917	K562	blood:	n/a	n/a
4	ATF1	chr10:42799538-42800192	K562	blood:	n/a	n/a
5	ATF1	chr10:42801380-42801410	K562	blood:	n/a	n/a
6	ATF1	chr10:42815222-42815574	K562	blood:	n/a	n/a
7	BACH1	chr10:42813274-42813746	K562	blood:	n/a	n/a
8	BATF	chr10:42843878-42844039	GM12878	blood:	n/a	chr10:42843938-42843949
9	BATF	chr10:42814968-42815467	GM12878	blood:	n/a	n/a
10	BATF	chr10:42801201-42801861	GM12878	blood:	n/a	n/a
11	BATF	chr10:42790411-42790908	GM12878	blood:	n/a	n/a
12	BATF	chr10:42734245-42734464	GM12878	blood:	n/a	n/a
13	BATF	chr10:42684802-42685128	GM12878	blood:	n/a	n/a
14	BATF	chr10:42792510-42793190	GM12878	blood:	n/a	n/a
15	BATF	chr10:42696631-42696866	GM12878	blood:	n/a	n/a
16	BATF	chr10:42704531-42704782	GM12878	blood:	n/a	chr10:42704640-42704651
17	BATF	chr10:42684889-42685225	GM12878	blood:	n/a	n/a
18	BATF	chr10:42816795-42818369	GM12878	blood:	n/a	n/a
19	BATF	chr10:42815938-42818365	GM12878	blood:	n/a	n/a
20	BATF	chr10:42775977-42776265	GM12878	blood:	n/a	n/a
21	BATF	chr10:42791008-42791549	GM12878	blood:	n/a	n/a
22	BATF	chr10:42794103-42794967	GM12878	blood:	n/a	n/a
23	BATF	chr10:42802384-42802603	GM12878	blood:	n/a	n/a
24	BATF	chr10:42791867-42792344	GM12878	blood:	n/a	n/a
25	BATF	chr10:42796760-42798052	GM12878	blood:	n/a	n/a
26	BATF	chr10:42791080-42791784	GM12878	blood:	n/a	n/a
27	BATF	chr10:42843892-42844051	GM12878	blood:	n/a	chr10:42843938-42843949
28	BATF	chr10:42799191-42800355	GM12878	blood:	n/a	n/a
29	BATF	chr10:42704442-42704772	GM12878	blood:	n/a	chr10:42704640-42704651
30	BATF	chr10:42799184-42800297	GM12878	blood:	n/a	n/a
31	BATF	chr10:42697926-42698033	GM12878	blood:	n/a	n/a
32	BATF	chr10:42691041-42691261	GM12878	blood:	n/a	n/a
33	BATF	chr10:42765314-42765560	GM12878	blood:	n/a	n/a
34	BATF	chr10:42790414-42790906	GM12878	blood:	n/a	n/a
35	BATF	chr10:42810326-42810760	GM12878	blood:	n/a	n/a
36	BATF	chr10:42794125-42794872	GM12878	blood:	n/a	n/a
37	BCL11A	chr10:42734310-42734513	GM12878	blood:	n/a	n/a
38	BCL11A	chr10:42704506-42704681	GM12878	blood:	n/a	n/a
39	BCL11A	chr10:42816269-42818366	GM12878	blood:	n/a	n/a
40	BCL11A	chr10:42738846-42739017	GM12878	blood:	n/a	n/a
41	BCL11A	chr10:42799172-42800370	GM12878	blood:	n/a	n/a
42	BCL11A	chr10:42794300-42794905	GM12878	blood:	n/a	n/a
43	BCL11A	chr10:42703088-42703254	GM12878	blood:	n/a	n/a
44	BCL11A	chr10:42790409-42790946	GM12878	blood:	n/a	n/a
45	BCL11A	chr10:42684825-42685022	GM12878	blood:	n/a	n/a
46	BCL11A	chr10:42684721-42685144	GM12878	blood:	n/a	n/a
47	BCL11A	chr10:42816771-42818395	GM12878	blood:	n/a	n/a
48	BCL11A	chr10:42704553-42704791	GM12878	blood:	n/a	n/a
49	BCL11A	chr10:42790997-42791796	GM12878	blood:	n/a	n/a
50	BCL11A	chr10:42705685-42705867	GM12878	blood:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:42863508-42863558	ECC-1	luminal epithelium:	n/a
2	chr10:42777375-42777425	GM06990	blood:	n/a
3	chr10:42863539-42863589	HPAEpiC	pulmonary alveolar:	n/a
4	chr10:42864633-42864683	CMK	blood:	n/a
5	chr10:42737582-42737632	MCF10A-Er-Src	breast:	n/a
6	chr10:42863444-42863494	HMEC	breast:	n/a
7	chr10:42737582-42737632	AG10803	skin:	n/a
8	chr10:42777375-42777425	AG04450	lung:	fetal
9	chr10:42859004-42859054	NHDF-neo	bronchial:	n/a
10	chr10:42738239-42738289	RPTEC	kidney:	n/a
11	chr10:42738815-42738865	AG04449	skin:	fetal
12	chr10:42863068-42863118	NT2-D1	testis:	n/a
13	chr10:42777525-42777575	SAEC	small airway:	n/a
14	chr10:42737582-42737632	HAEpiC	amniotic membrane:	n/a
15	chr10:42863594-42863644	GM12892	blood:	n/a
16	chr10:42738815-42738865	AG09309	skin:	n/a
17	chr10:42863173-42863223	CMK	blood:	n/a
18	chr10:42859004-42859054	PrEC	prostate:	n/a
19	chr10:42738239-42738289	HRE	kidney:	n/a
20	chr10:42862876-42862926	IMR90	lung:	fetal
21	chr10:42864633-42864683	H1-hESC	embryonic stem cell:	embryo
22	chr10:42862876-42862926	H1-hESC	embryonic stem cell:	embryo
23	chr10:42862978-42863028	AoSMC	blood vessel:	n/a
24	chr10:42737322-42737372	H1-hESC	embryonic stem cell:	embryo
25	chr10:42777525-42777575	MCF-7	breast:	n/a
26	chr10:42862978-42863028	ovcar-3	ovarian:	n/a
27	chr10:42863508-42863558	SAEC	small airway:	n/a
28	chr10:42738239-42738289	IMR90	lung:	fetal
29	chr10:42737582-42737632	SK-N-SH	brain:	n/a
30	chr10:42738815-42738865	Caco-2	colon:	n/a
31	chr10:42777525-42777575	CMK	blood:	n/a
32	chr10:42737322-42737372	Hela-S3	cervix:	n/a
33	chr10:42863508-42863558	HCF	heart:	n/a
34	chr10:42738815-42738865	PANC-1	pancreas:	n/a
35	chr10:42738538-42738588	HEEpiC	esophagus:	n/a
36	chr10:42864633-42864683	BJ	skin:	n/a
37	chr10:42737139-42737189	BJ	skin:	n/a
38	chr10:42863550-42863600	MCF-7	breast:	n/a
39	chr10:42863508-42863558	BE2_C	brain:	n/a
40	chr10:42862876-42862926	HCF	heart:	n/a
41	chr10:42739066-42739116	AG04449	skin:	fetal
42	chr10:42738815-42738865	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:42737582-42737632	HUVEC	blood vessel:	n/a
44	chr10:42862876-42862926	SKMC	muscle:	n/a
45	chr10:42737139-42737189	NB4	blood:	n/a
46	chr10:42863068-42863118	LNCaP	prostate:	n/a
47	chr10:42777403-42777453	SK-N-MC	brain:	n/a
48	chr10:42738538-42738588	HAEpiC	amniotic membrane:	n/a
49	chr10:42745966-42746016	HCF	heart:	n/a
50	chr10:42777525-42777575	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:42822722..42825307-chr10:42828970..42830910,2	K562	blood:
2	chr10:42843787..42846463-chr10:42857739..42859504,2	K562	blood:
3	chr10:42843787..42846463-chr10:42856590..42859504,3	K562	blood:
4	chr10:42861377..42864864-chr10:42876467..42879026,3	K562	blood:
5	chr10:42860335..42863039-chr10:43132551..43135299,2	K562	blood:
6	chr10:42822722..42825307-chr10:42828970..42830910,2	K562	blood:
7	chr10:42843787..42846463-chr10:42856590..42859504,3	K562	blood:
8	chr10:42846704..42848638-chr10:42856458..42859194,2	K562	blood:
9	chr10:42851804..42854724-chr10:42857105..42858652,2	K562	blood:
10	chr10:42851804..42854724-chr10:42857105..42858652,2	K562	blood:
11	chr10:42843787..42846463-chr10:42857739..42859504,2	K562	blood:
12	chr10:42739123..42739644-chr10:101379768..101380454,2	HCT-116	colon:
13	chr10:42673795..42674377-chr10:42765091..42765784,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMS1-9	chr10:42687963-42689514	NONHSAT012855
2	lnc-CCNYL2-5	chr10:42795737-42796013	NONHSAT012863
3	lnc-CCNYL2-5	chr10:42794471-42794553	NONHSAT012863
4	lnc-BMS1-6	chr10:42791078-42791322	NONHSAT012862
5	lnc-BMS1-9	chr10:42686975-42687136	NONHSAT012855
6	lnc-CCNYL2-6	chr10:42775182-42777267	NONHSAT012861
7	lnc-BMS1-8	chr10:42705438-42705831	NONHSAT012856
8	lnc-BMS1-7	chr10:42737930-42738014	NONHSAT012859
9	lnc-BMS1-7	chr10:42746444-42746645	NONHSAT012859
10	lnc-CCNYL2-5	chr10:42796822-42796961	NONHSAT012863

No data

Variant related genes	Relation type
ENSG00000264398	TF binding region
PABPC1P8	TF binding region
ENSG00000271650	TF binding region
ENSG00000215146	TF binding region
ENSG00000264398	CpG island
PABPC1P8	CpG island
ENSG00000271650	CpG island
ENSG00000215146	CpG island
ENSG00000215146	chromatin interactions
ENSG00000272373	chromatin interactions
ENSG00000155287	chromatin interactions
ENSG00000196693	chromatin interactions

Extended variants
information (count: 6792 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6792 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78473109	chr10:42687055-42687056	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs572040421	chr10:42687061-42687062	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs534628163	chr10:42687072-42687073	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs554587981	chr10:42687073-42687074	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs117750073	chr10:42687095-42687096	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs184925088	chr10:42687096-42687097	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs543314426	chr10:42687135-42687136	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs528197268	chr10:42687976-42687977	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs548266256	chr10:42687991-42687992	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs534683181	chr10:42688004-42688005	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs183590497	chr10:42688013-42688014	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs187475242	chr10:42688040-42688041	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs4625409	chr10:42688042-42688043	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs192477516	chr10:42688057-42688058	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs556663381	chr10:42688090-42688091	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs570362847	chr10:42688146-42688147	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs12414128	chr10:42688176-42688177	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs543744041	chr10:42688178-42688179	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs556937454	chr10:42688219-42688220	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs572261791	chr10:42688242-42688243	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs541138928	chr10:42688243-42688244	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs200338784	chr10:42688283-42688284	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs376672325	chr10:42688308-42688309	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs574568660	chr10:42688314-42688315	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs184842699	chr10:42688376-42688377	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs563497719	chr10:42688380-42688381	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs186504769	chr10:42688400-42688401	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs192721300	chr10:42688401-42688402	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs559596800	chr10:42688406-42688407	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs184637668	chr10:42688469-42688470	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs548401740	chr10:42688499-42688500	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs568190363	chr10:42688558-42688559	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs530507815	chr10:42688559-42688560	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs79404313	chr10:42688628-42688629	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs375390396	chr10:42688650-42688651	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs56908850	chr10:42688651-42688652	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs189910339	chr10:42688666-42688667	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs570326556	chr10:42688695-42688696	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs372528391	chr10:42688717-42688718	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs549772589	chr10:42688723-42688724	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs12260937	chr10:42688804-42688805	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs527815776	chr10:42688864-42688865	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs566026781	chr10:42688870-42688871	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs12257517	chr10:42688911-42688912	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs554723862	chr10:42688947-42688948	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs574607029	chr10:42688963-42688964	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs543523050	chr10:42688968-42688969	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs189264519	chr10:42688982-42688983	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs59955462	chr10:42688983-42688984	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs530186852	chr10:42689008-42689009	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Lung cancer	18438408	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
Breast cancer	21509527	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	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
Obesity	20622171	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD

Chromatin state (count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:42712200-42712400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr10:42712200-42712800	Enhancers	HepG2	liver
3	chr10:42712400-42712800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr10:42712400-42712800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:42712400-42712800	Enhancers	Adipose Nuclei	Adipose
6	chr10:42712400-42712800	Enhancers	Aorta	Aorta
7	chr10:42712400-42712800	Enhancers	Hela-S3	cervix
8	chr10:42725600-42726200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr10:42725600-42726200	Enhancers	Pancreas	Pancrea
10	chr10:42725600-42726800	ZNF genes & repeats	Esophagus	oesophagus
11	chr10:42726200-42726800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr10:42726800-42728200	Weak transcription	Esophagus	oesophagus
13	chr10:42728200-42730600	Enhancers	Esophagus	oesophagus
14	chr10:42728800-42729400	ZNF genes & repeats	Spleen	Spleen
15	chr10:42728800-42730400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr10:42729000-42729400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr10:42729400-42732200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:42732200-42732400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr10:42732200-42732400	Enhancers	Gastric	stomach
20	chr10:42732400-42742600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr10:42736600-42737000	Weak transcription	HSMMtube	muscle
22	chr10:42737000-42737200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
23	chr10:42737000-42737200	Active TSS	HSMM	muscle
24	chr10:42737000-42737400	Enhancers	Primary hematopoietic stem cells	blood
25	chr10:42737000-42737400	Active TSS	HMEC	breast
26	chr10:42737000-42737400	ZNF genes & repeats	HSMMtube	muscle
27	chr10:42737000-42737400	Bivalent Enhancer	NHEK	skin
28	chr10:42737000-42737600	Enhancers	Osteobl	bone
29	chr10:42737000-42738400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr10:42737000-42738400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr10:42737200-42737400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
32	chr10:42737200-42737400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
33	chr10:42737200-42737400	Enhancers	Brain Substantia Nigra	brain
34	chr10:42737200-42737400	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr10:42737200-42737400	Flanking Active TSS	HSMM	muscle
36	chr10:42737200-42737400	ZNF genes & repeats	NH-A	brain
37	chr10:42737200-42737600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
38	chr10:42737200-42738200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
39	chr10:42737400-42738000	Weak transcription	HSMM	muscle
40	chr10:42737400-42739000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr10:42737600-42737800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr10:42737600-42737800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr10:42737600-42738000	Active TSS	Esophagus	oesophagus
44	chr10:42737600-42738000	Active TSS	Pancreas	Pancrea
45	chr10:42737600-42738000	Bivalent/Poised TSS	Right Ventricle	heart
46	chr10:42737600-42738000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
47	chr10:42737600-42738400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr10:42737600-42738400	Active TSS	Colon Smooth Muscle	Colon
49	chr10:42737600-42738800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr10:42737600-42739200	Active TSS	Ovary	ovary

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