Variant report

Variant	nsv947892
Chromosome Location	chr10:43358233-43368929
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43366883-43366989	HepG2	liver:	n/a	n/a
2	ATF1	chr10:43362943-43363029	K562	blood:	n/a	n/a
3	BACH1	chr10:43360208-43360382	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:43362173-43362398	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:43361855-43361897	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr10:43365040-43365394	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:43366623-43366760	K562	blood:	n/a	chr10:43366705-43366726 chr10:43366712-43366721
8	BHLHE40	chr10:43366559-43366917	HepG2	liver:	n/a	chr10:43366705-43366726 chr10:43366712-43366721
9	BHLHE40	chr10:43362265-43362383	K562	blood:	n/a	n/a
10	CEBPB	chr10:43362317-43362460	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr10:43366799-43367005	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr10:43362281-43362350	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr10:43362263-43362300	K562	blood:	n/a	n/a
14	CHD2	chr10:43362228-43362397	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr10:43360100-43360250	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr10:43362192-43362437	A549	lung:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
17	CTCF	chr10:43362108-43362477	K562	blood:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
18	CTCF	chr10:43362220-43362370	SK-N-SH_RA	brain:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
19	CTCF	chr10:43362060-43362210	NHEK	skin:	n/a	n/a
20	CTCF	chr10:43360164-43360355	Fibrobl	skin:	n/a	chr10:43360279-43360295 chr10:43360283-43360291
21	CTCF	chr10:43360320-43360470	MCF-7	breast:	n/a	n/a
22	CTCF	chr10:43360180-43360470	AG09319	gingival:	n/a	chr10:43360279-43360295 chr10:43360283-43360291
23	CTCF	chr10:43361980-43362052	Medullo	brain:	n/a	n/a
24	CTCF	chr10:43361917-43362052	Gliobla	brain:	n/a	n/a
25	CTCF	chr10:43359372-43359462	LNCaP	prostate:	n/a	n/a
26	CTCF	chr10:43362188-43362380	SK-N-SH_RA	brain:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
27	CTCF	chr10:43362260-43362410	Hela-S3	cervix:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
28	CTCF	chr10:43361780-43361930	NHLF	lung:	n/a	n/a
29	CTCF	chr10:43362098-43362480	GM12878	blood:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
30	CTCF	chr10:43360120-43360270	HCM	heart:	n/a	n/a
31	CTCF	chr10:43362140-43362290	A549	lung:	n/a	n/a
32	CTCF	chr10:43366880-43367030	AG10803	skin:	n/a	n/a
33	CTCF	chr10:43362240-43362390	AG10803	skin:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
34	CTCF	chr10:43362220-43362370	GM12875	blood:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
35	CTCF	chr10:43362159-43362425	GM19240	blood:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
36	CTCF	chr10:43360144-43360368	MCF-7	breast:	n/a	chr10:43360279-43360295 chr10:43360283-43360291
37	CTCF	chr10:43360080-43360230	HAc	cerebellar:	n/a	n/a
38	CTCF	chr10:43362171-43362426	Kidney_OC	kidney:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
39	CTCF	chr10:43361740-43361890	GM06990	blood:	n/a	n/a
40	CTCF	chr10:43360100-43360250	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr10:43360160-43360310	HepG2	liver:	n/a	chr10:43360279-43360295 chr10:43360283-43360291
42	CTCF	chr10:43360180-43360330	HMEC	breast:	n/a	chr10:43360279-43360295 chr10:43360283-43360291
43	CTCF	chr10:43360320-43360470	WI-38	lung:	n/a	n/a
44	CTCF	chr10:43360297-43360302	GM12891	blood:	n/a	n/a
45	CTCF	chr10:43360200-43360256	GM10266	blood:	n/a	n/a
46	CTCF	chr10:43362260-43362410	HCT-116	colon:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
47	CTCF	chr10:43360180-43360330	NHEK	skin:	n/a	chr10:43360279-43360295 chr10:43360283-43360291
48	CTCF	chr10:43360144-43360414	GM12878	blood:	n/a	chr10:43360279-43360295 chr10:43360283-43360291
49	CTCF	chr10:43360080-43360230	GM12872	blood:	n/a	n/a
50	CTCF	chr10:43361962-43362029	Spleen_OC	spleen:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43361339-43361389	H1-hESC	embryonic stem cell:	embryo
2	chr10:43362076-43362126	GM12891	blood:	n/a
3	chr10:43361553-43361603	HAEpiC	amniotic membrane:	n/a
4	chr10:43361339-43361389	H1-hESC	embryonic stem cell:	embryo
5	chr10:43362076-43362126	GM12891	blood:	n/a
6	chr10:43361553-43361603	HAEpiC	amniotic membrane:	n/a
7	chr10:43365572-43365622	SKMC	muscle:	n/a
8	chr10:43361605-43361655	BE2_C	brain:	n/a
9	chr10:43362626-43362676	GM06990	blood:	n/a
10	chr10:43361618-43361668	GM19239	blood:	n/a
11	chr10:43361261-43361311	GM19239	blood:	n/a
12	chr10:43362202-43362252	Jurkat	blood:	n/a
13	chr10:43365572-43365622	Hepatocyte	liver:	n/a
14	chr10:43361339-43361389	HRCEpiC	kidney:	n/a
15	chr10:43358370-43358420	A549	lung:	n/a
16	chr10:43362202-43362252	BJ	skin:	n/a
17	chr10:43361553-43361603	NHDF-neo	bronchial:	n/a
18	chr10:43361553-43361603	HMEC	breast:	n/a
19	chr10:43365572-43365622	HUVEC	blood vessel:	n/a
20	chr10:43361339-43361389	NHBE	bronchial:	n/a
21	chr10:43360327-43360377	NB4	blood:	n/a
22	chr10:43361605-43361655	NB4	blood:	n/a
23	chr10:43362076-43362126	HAEpiC	amniotic membrane:	n/a
24	chr10:43361261-43361311	HCF	heart:	n/a
25	chr10:43360327-43360377	SK-N-MC	brain:	n/a
26	chr10:43362076-43362126	ECC-1	luminal epithelium:	n/a
27	chr10:43361618-43361668	ECC-1	luminal epithelium:	n/a
28	chr10:43362626-43362676	NHDF-neo	bronchial:	n/a
29	chr10:43361618-43361668	Jurkat	blood:	n/a
30	chr10:43365572-43365622	HCF	heart:	n/a
31	chr10:43361618-43361668	HRPEpiC	eye:	n/a
32	chr10:43362202-43362252	Hepatocyte	liver:	n/a
33	chr10:43361553-43361603	HL-60	blood:	n/a
34	chr10:43358370-43358420	HCF	heart:	n/a
35	chr10:43362076-43362126	SAEC	small airway:	n/a
36	chr10:43360327-43360377	HMEC	breast:	n/a
37	chr10:43362202-43362252	HL-60	blood:	n/a
38	chr10:43362076-43362126	GM19239	blood:	n/a
39	chr10:43358370-43358420	AG04449	skin:	fetal
40	chr10:43361618-43361668	HEEpiC	esophagus:	n/a
41	chr10:43362684-43362734	NT2-D1	testis:	n/a
42	chr10:43358370-43358420	HUVEC	blood vessel:	n/a
43	chr10:43362202-43362252	HRCEpiC	kidney:	n/a
44	chr10:43361553-43361603	HepG2	liver:	n/a
45	chr10:43362370-43362420	AG09309	skin:	n/a
46	chr10:43361339-43361389	HAEpiC	amniotic membrane:	n/a
47	chr10:43362202-43362252	NT2-D1	testis:	n/a
48	chr10:43362626-43362676	GM12892	blood:	n/a
49	chr10:43362626-43362676	NB4	blood:	n/a
50	chr10:43362076-43362126	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr10:43359656..43362276-chr10:43538559..43540315,2	MCF-7	breast:
2	chr10:43355311..43356829-chr10:43360308..43362900,2	MCF-7	breast:
3	chr10:43361928..43362761-chr10:43600658..43601529,2	MCF-7	breast:
4	chr10:43361913..43362690-chr10:43470789..43471679,3	MCF-7	breast:
5	chr10:43360364..43363685-chr10:43571830..43575400,3	MCF-7	breast:
6	chr10:43360554..43363791-chr10:43570974..43576100,9	MCF-7	breast:
7	chr10:43365868..43366659-chr10:43470638..43471752,5	MCF-7	breast:
8	chr10:43363801..43367756-chr10:43571423..43575718,4	MCF-7	breast:
9	chr10:43364725..43366400-chr10:43449208..43451181,2	MCF-7	breast:
10	chr10:43361133..43364035-chr10:43632950..43635001,2	MCF-7	breast:
11	chr10:43360509..43362298-chr10:43627787..43629550,2	MCF-7	breast:
12	chr10:43361854..43362671-chr10:43600633..43601533,4	K562	blood:
13	chr10:43361782..43362789-chr10:43574108..43574983,3	K562	blood:
14	chr10:43368762..43369411-chr10:43606065..43606957,2	MCF-7	breast:
15	chr10:43361867..43362389-chr10:43470791..43471531,2	K562	blood:
16	chr10:43365921..43366623-chr10:43521643..43522303,3	MCF-7	breast:
17	chr10:43361921..43363073-chr10:43574052..43574909,5	MCF-7	breast:
18	chr10:43363351..43366348-chr2:91758287..91761339,3	K562	blood:
19	chr10:43359833..43360692-chr10:43600708..43601545,3	MCF-7	breast:
20	chr10:43362412..43363000-chr10:43573894..43574641,2	MCF-7	breast:
21	chr10:43361871..43362799-chr10:43470867..43471733,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMS1-1	chr10:43366969-43367130	XLOC_008465
2	lnc-BMS1-1	chr10:43367957-43369508	XLOC_008465

Variant related genes	Relation type
ENSG00000234944	TF binding region
ENSG00000234944	CpG island
ENSG00000169826	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000273008	chromatin interactions

Extended variants
information (count: 589 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117102481	chr10:43358246-43358247	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs544753504	chr10:43358251-43358252	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs527533447	chr10:43358277-43358278	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs2796557	chr10:43358279-43358280	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs73256259	chr10:43358310-43358311	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs542520658	chr10:43358323-43358324	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs560802798	chr10:43358349-43358350	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs2795510	chr10:43358371-43358372	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs540658347	chr10:43358380-43358381	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs111280941	chr10:43358386-43358387	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs112281998	chr10:43358423-43358424	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs73256260	chr10:43358444-43358445	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs181028704	chr10:43358453-43358454	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs550765080	chr10:43358478-43358479	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs563085382	chr10:43358499-43358500	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs530272420	chr10:43358567-43358568	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs549437778	chr10:43358570-43358571	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs548799264	chr10:43358597-43358598	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs185448961	chr10:43358690-43358691	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs534209853	chr10:43358707-43358708	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs146001620	chr10:43358709-43358710	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs788288	chr10:43358730-43358731	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538425344	chr10:43358743-43358744	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs558343680	chr10:43358748-43358749	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs556741022	chr10:43358752-43358753	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs565427801	chr10:43358768-43358769	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs190204346	chr10:43358769-43358770	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs182844432	chr10:43358795-43358796	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs187264793	chr10:43358828-43358829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540128938	chr10:43358829-43358830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191687304	chr10:43358840-43358841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183872557	chr10:43358867-43358868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544699284	chr10:43358896-43358897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563020007	chr10:43358929-43358930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534459929	chr10:43358930-43358931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553838027	chr10:43358996-43358997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76436021	chr10:43359052-43359053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530210664	chr10:43359100-43359101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548832037	chr10:43359132-43359133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs72782079	chr10:43359133-43359134	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs2796556	chr10:43359170-43359171	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs188817281	chr10:43359254-43359255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576013231	chr10:43359336-43359337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192692310	chr10:43359338-43359339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538209327	chr10:43359373-43359374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs3905141	chr10:43359390-43359391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs9783200	chr10:43359419-43359420	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs535922204	chr10:43359493-43359494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554366158	chr10:43359497-43359498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566514721	chr10:43359542-43359543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
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
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
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43347600-43360000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:43355000-43360000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr10:43356800-43361600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr10:43357400-43361200	Weak transcription	HMEC	breast
5	chr10:43358200-43358400	Enhancers	Primary hematopoietic stem cells	blood
6	chr10:43358200-43358400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr10:43358200-43358800	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr10:43358200-43358800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:43358400-43361400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr10:43358600-43359600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr10:43358800-43359800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr10:43358800-43360800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:43359600-43360400	Enhancers	Primary hematopoietic stem cells	blood
14	chr10:43359800-43360400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
15	chr10:43360000-43360200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr10:43360000-43360200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr10:43360000-43360200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr10:43360000-43360200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
19	chr10:43360000-43360200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr10:43360000-43360200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr10:43360000-43360200	Enhancers	Pancreas	Pancrea
22	chr10:43360000-43360200	Bivalent/Poised TSS	HepG2	liver
23	chr10:43360000-43360400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
24	chr10:43360000-43360400	Bivalent/Poised TSS	Hela-S3	cervix
25	chr10:43360000-43360400	Enhancers	NHEK	skin
26	chr10:43360000-43360600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr10:43360000-43360800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr10:43360200-43360400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr10:43360200-43360400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr10:43360200-43360400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr10:43360200-43361600	Weak transcription	Pancreas	Pancrea
32	chr10:43360400-43360800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr10:43360800-43361000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr10:43360800-43361200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr10:43360800-43361200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr10:43361200-43361400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
37	chr10:43361200-43361400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr10:43361200-43361400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr10:43361200-43361400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr10:43361200-43361600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr10:43361200-43361600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
42	chr10:43361200-43361600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr10:43361200-43361600	Enhancers	HMEC	breast
44	chr10:43361200-43361800	Bivalent Enhancer	Fetal Brain Male	brain
45	chr10:43361200-43362000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr10:43361200-43362000	Bivalent Enhancer	Placenta	Placenta
47	chr10:43361400-43361600	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr10:43361400-43361600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr10:43361400-43361800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
50	chr10:43361400-43361800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood

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