Variant report

Variant	nsv1041825
Chromosome Location	chr10:43450288-43487986
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	ATF1	chr10:43474747-43475125	K562	blood:	n/a	n/a
2	ATF1	chr10:43474055-43474377	K562	blood:	n/a	n/a
3	BACH1	chr10:43455879-43456257	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr10:43455972-43456235	GM12878	blood:	n/a	n/a
5	BHLHE40	chr10:43476829-43477169	K562	blood:	n/a	chr10:43476970-43476986
6	BHLHE40	chr10:43484487-43484837	K562	blood:	n/a	n/a
7	CCNT2	chr10:43476863-43477053	K562	blood:	n/a	n/a
8	CEBPB	chr10:43456810-43457012	K562	blood:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
9	CEBPB	chr10:43468559-43468690	K562	blood:	n/a	chr10:43468625-43468636 chr10:43468624-43468637
10	CEBPB	chr10:43467355-43467475	IMR90	lung:	n/a	n/a
11	CEBPB	chr10:43468469-43468786	HepG2	liver:	n/a	chr10:43468625-43468636 chr10:43468624-43468637
12	CEBPB	chr10:43477134-43477208	K562	blood:	n/a	n/a
13	CEBPB	chr10:43474862-43474980	K562	blood:	n/a	n/a
14	CEBPB	chr10:43456772-43457109	A549	lung:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
15	CEBPB	chr10:43456763-43457109	IMR90	lung:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
16	CEBPB	chr10:43456879-43457110	Hela-S3	cervix:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
17	CEBPB	chr10:43456758-43457107	HepG2	liver:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
18	CHD2	chr10:43471209-43471243	HepG2	liver:	n/a	n/a
19	CTCF	chr10:43452974-43452993	GM10248	blood:	n/a	n/a
20	CTCF	chr10:43471134-43471359	H1-hESC	embryonic stem cell:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
21	CTCF	chr10:43455971-43456059	NHEK	skin:	n/a	n/a
22	CTCF	chr10:43471167-43471341	GM12891	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
23	CTCF	chr10:43471160-43471310	GM12878	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
24	CTCF	chr10:43471123-43471391	K562	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
25	CTCF	chr10:43471140-43471290	AG04449	skin:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
26	CTCF	chr10:43455973-43456063	MCF-7	breast:	n/a	n/a
27	CTCF	chr10:43453483-43453514	GM12891	blood:	n/a	n/a
28	CTCF	chr10:43471129-43471397	Gliobla	brain:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
29	CTCF	chr10:43471180-43471329	ProgFib	skin:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
30	CTCF	chr10:43470740-43470890	NB4	blood:	n/a	n/a
31	CTCF	chr10:43453320-43453470	HL-60	blood:	n/a	n/a
32	CTCF	chr10:43455966-43455969	NHEK	skin:	n/a	n/a
33	CTCF	chr10:43471180-43471330	GM12864	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
34	CTCF	chr10:43471200-43471350	HepG2	liver:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
35	CTCF	chr10:43471180-43471276	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr10:43471072-43471375	HepG2	liver:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
37	CTCF	chr10:43471087-43471441	K562	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
38	CTCF	chr10:43453461-43453521	GM12892	blood:	n/a	n/a
39	CTCF	chr10:43457940-43458090	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr10:43471220-43471370	GM12866	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
41	CTCF	chr10:43471192-43471328	GM19238	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
42	CTCF	chr10:43471145-43471371	A549	lung:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
43	CTCF	chr10:43471072-43471434	K562	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
44	CTCF	chr10:43471160-43471310	GM12866	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
45	CTCF	chr10:43471117-43471401	MCF-7	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
46	CTCF	chr10:43453414-43453499	Lung_OC	lung:	n/a	n/a
47	CTCF	chr10:43471133-43471394	NHEK	skin:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
48	CTCF	chr10:43455760-43455910	RPTEC	kidney:	n/a	n/a
49	CTCF	chr10:43453439-43453551	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:43470874-43471577	MCF-7	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286

No.	Distal block	Cell Line	Cell type
1	chr10:43454448..43456264-chr10:43474294..43477157,2	MCF-7	breast:
2	chr10:43469169..43471779-chr10:43471792..43473949,2	K562	blood:
3	chr10:43365868..43366659-chr10:43470638..43471752,5	MCF-7	breast:
4	chr10:43454969..43457476-chr10:43464603..43467508,2	MCF-7	breast:
5	chr10:43486095..43489357-chr10:43490017..43492485,3	MCF-7	breast:
6	chr10:43471160..43472154-chr11:102217419..102218246,2	NB4	blood:
7	chr10:43471183..43472148-chr4:106629910..106630418,2	NB4	blood:
8	chr10:43477135..43480872-chr10:43482623..43485089,4	MCF-7	breast:
9	chr10:43471330..43471857-chr3:38035458..38036022,2	NB4	blood:
10	chr10:43458559..43459070-chr17:7387320..7387822,2	NB4	blood:
11	chr10:43482866..43485744-chr10:43490374..43493373,2	K562	blood:
12	chr10:43472378..43475581-chr10:43520718..43522410,3	MCF-7	breast:
13	chr10:43467866..43472352-chr10:43571131..43575180,5	MCF-7	breast:
14	chr10:43442278..43444933-chr10:43480874..43482921,2	K562	blood:
15	chr10:43452048..43454806-chr10:43520323..43522084,2	MCF-7	breast:
16	chr10:43463562..43467082-chr10:43469575..43473842,3	MCF-7	breast:
17	chr10:43454969..43457476-chr10:43464603..43467508,2	MCF-7	breast:
18	chr1:113932116..113933106-chr10:43470154..43470896,2	NB4	blood:
19	chr10:43361871..43362799-chr10:43470867..43471733,6	MCF-7	breast:
20	chr10:43481086..43483555-chr10:43520776..43523098,2	MCF-7	breast:
21	chr10:43450142..43452389-chr10:43455226..43458611,3	K562	blood:
22	chr10:43469169..43471779-chr10:43471792..43473949,2	K562	blood:
23	chr10:43450142..43452389-chr10:43455226..43458611,3	K562	blood:
24	chr10:43470043..43470710-chr4:7069530..7070337,2	NB4	blood:
25	chr10:43448104..43449836-chr10:43453416..43456002,2	MCF-7	breast:
26	chr10:43454488..43457151-chr10:43458866..43460532,2	K562	blood:
27	chr10:43369343..43371320-chr10:43469616..43472165,2	MCF-7	breast:
28	chr10:43474227..43476529-chr10:43479652..43481353,2	MCF-7	breast:
29	chr10:43465926..43467640-chr10:43469651..43471316,2	K562	blood:
30	chr10:43454488..43457151-chr10:43458866..43460532,2	K562	blood:
31	chr10:43450805..43453524-chr10:43455350..43458252,2	MCF-7	breast:
32	chr10:43487519..43490099-chr10:43491819..43493663,2	MCF-7	breast:
33	chr10:43477135..43480872-chr10:43482623..43485089,4	MCF-7	breast:
34	chr10:43423641..43426071-chr10:43452071..43454009,2	MCF-7	breast:
35	chr10:43472744..43475645-chr10:43482853..43485433,2	K562	blood:
36	chr10:43469610..43472857-chr10:43520371..43524809,5	MCF-7	breast:
37	chr10:43484291..43485932-chr10:43488466..43491187,2	MCF-7	breast:
38	chr10:43457137..43457637-chr11:95522694..95523216,2	NB4	blood:
39	chr10:43450408..43453024-chr10:43497080..43499917,2	K562	blood:
40	chr10:43465926..43467640-chr10:43469651..43471316,2	K562	blood:
41	chr10:43364725..43366400-chr10:43449208..43451181,2	MCF-7	breast:
42	chr10:43474536..43476774-chr10:43520389..43522895,3	MCF-7	breast:
43	chr10:43470988..43471723-chr10:43574194..43574824,2	MCF-7	breast:
44	chr10:43472744..43475645-chr10:43482853..43485433,2	K562	blood:
45	chr10:43361867..43362389-chr10:43470791..43471531,2	K562	blood:
46	chr10:43361913..43362690-chr10:43470789..43471679,3	MCF-7	breast:
47	chr10:43472048..43472812-chr11:819441..820070,2	NB4	blood:
48	chr10:43450805..43453524-chr10:43455350..43458252,2	MCF-7	breast:
49	chr10:43474227..43476529-chr10:43479652..43481353,2	MCF-7	breast:
50	chr10:43471587..43474099-chr10:43476210..43479281,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RET-3	chr10:43486575-43486975	ucscGeneNc_uc001jba_2
2	lnc-RET-2	chr10:43481122-43481247	NONHSAT012938
3	lnc-RET-3	chr10:43487172-43487532	ucscGeneNc_uc001jba_2
4	lnc-RET-3	chr10:43487762-43487899	ucscGeneNc_uc001jba_2
5	lnc-RET-2	chr10:43482124-43482459	NONHSAT012938
6	lnc-RASGEF1A-1	chr10:43476816-43476955	XLOC_008790
7	lnc-RASGEF1A-1	chr10:43474465-43474547	XLOC_008790
8	lnc-RASGEF1A-1	chr10:43475731-43476007	XLOC_008790

Variant related genes	Relation type
ENSG00000229630	TF binding region
ENSG00000165731	chromatin interactions
ENSG00000109519	chromatin interactions
ENSG00000110330	chromatin interactions
ENSG00000077458	chromatin interactions
ENSG00000229630	chromatin interactions
ENSG00000166037	chromatin interactions
ENSG00000181222	chromatin interactions
ENSG00000136059	chromatin interactions
ENSG00000138785	chromatin interactions
ENSG00000138780	chromatin interactions
ENSG00000263795	chromatin interactions
ENSG00000174282	chromatin interactions

Extended variants
information (count: 1564 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1564 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569640420	chr10:43450292-43450293	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs141278689	chr10:43450354-43450355	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs548857246	chr10:43450490-43450491	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs567571267	chr10:43450523-43450524	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs77986482	chr10:43450535-43450536	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs552830333	chr10:43450541-43450542	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs149836321	chr10:43450548-43450549	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs189881105	chr10:43450602-43450603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557076574	chr10:43450605-43450606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113243967	chr10:43450633-43450634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575610795	chr10:43450645-43450646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74905090	chr10:43450681-43450682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145812842	chr10:43450698-43450699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573497363	chr10:43450724-43450725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540961624	chr10:43450736-43450737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs118148851	chr10:43450737-43450738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532997596	chr10:43450748-43450749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563398498	chr10:43450760-43450761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530492705	chr10:43450772-43450773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549174304	chr10:43450781-43450782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533661864	chr10:43450829-43450830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567380753	chr10:43450889-43450890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545814634	chr10:43450933-43450934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539888964	chr10:43450995-43450996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143811194	chr10:43450999-43451000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528837441	chr10:43451022-43451023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546539577	chr10:43451076-43451077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571202183	chr10:43451123-43451124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538660666	chr10:43451135-43451136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557029147	chr10:43451162-43451163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs61845262	chr10:43451185-43451186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs536315021	chr10:43451209-43451210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115600093	chr10:43451218-43451219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs118024813	chr10:43451257-43451258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540820304	chr10:43451281-43451282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565586823	chr10:43451315-43451316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117271272	chr10:43451365-43451366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545043591	chr10:43451371-43451372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35920288	chr10:43451391-43451392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7896997	chr10:43451398-43451399	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs530508439	chr10:43451422-43451423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3128734	chr10:43451430-43451431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs561032820	chr10:43451492-43451493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573926234	chr10:43451516-43451517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138519068	chr10:43451539-43451540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375859094	chr10:43451563-43451564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546351477	chr10:43451564-43451565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571214436	chr10:43451590-43451591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532247491	chr10:43451624-43451625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182646358	chr10:43451681-43451682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43447600-43450600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
2	chr10:43447600-43455800	Weak transcription	Left Ventricle	heart
3	chr10:43448600-43456200	Weak transcription	Right Ventricle	heart
4	chr10:43449200-43451800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr10:43449800-43451000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr10:43450200-43450400	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr10:43451800-43452000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:43452800-43453000	ZNF genes & repeats	HSMMtube	muscle
9	chr10:43453000-43455800	Weak transcription	HSMMtube	muscle
10	chr10:43453400-43459200	Enhancers	Fetal Muscle Leg	muscle
11	chr10:43454400-43455000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr10:43454600-43454800	Weak transcription	Psoas Muscle	Psoas
13	chr10:43454800-43455000	Enhancers	Psoas Muscle	Psoas
14	chr10:43454800-43458600	Enhancers	Spleen	Spleen
15	chr10:43454800-43458800	Enhancers	Fetal Muscle Trunk	muscle
16	chr10:43455000-43455800	Weak transcription	Psoas Muscle	Psoas
17	chr10:43455200-43457600	Enhancers	HMEC	breast
18	chr10:43455400-43456600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr10:43455400-43457400	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr10:43455400-43457600	Enhancers	NHEK	skin
21	chr10:43455600-43456800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr10:43455600-43458000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr10:43455800-43456400	Enhancers	Muscle Satellite Cultured Cells	--
24	chr10:43455800-43456400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr10:43455800-43456600	Enhancers	HSMMtube	muscle
26	chr10:43455800-43457000	Enhancers	HSMM	muscle
27	chr10:43455800-43458000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr10:43455800-43458400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr10:43455800-43458400	Enhancers	Placenta	Placenta
30	chr10:43455800-43458600	Enhancers	Left Ventricle	heart
31	chr10:43455800-43458600	Enhancers	Psoas Muscle	Psoas
32	chr10:43455800-43458600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
33	chr10:43455800-43460200	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr10:43456000-43456400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr10:43456000-43458200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr10:43456000-43458600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr10:43456000-43458600	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr10:43456200-43456600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr10:43456200-43457800	Enhancers	Right Atrium	heart
40	chr10:43456200-43458400	Enhancers	Right Ventricle	heart
41	chr10:43456400-43456600	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr10:43456400-43457000	Enhancers	Pancreas	Pancrea
43	chr10:43456400-43457400	Enhancers	Fetal Stomach	stomach
44	chr10:43456400-43457600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr10:43456400-43459400	Enhancers	Adipose Nuclei	Adipose
46	chr10:43456600-43457000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr10:43456600-43457000	Weak transcription	HSMMtube	muscle
48	chr10:43456600-43461800	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr10:43456800-43458000	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr10:43456800-43459000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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