Variant report

Variant	nsv895077
Chromosome Location	chr10:43452436-43506861
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	chr10:43468559-43468690	K562	blood:	n/a	chr10:43468625-43468636 chr10:43468624-43468637
9	CEBPB	chr10:43456772-43457109	A549	lung:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
10	CEBPB	chr10:43467355-43467475	IMR90	lung:	n/a	n/a
11	CEBPB	chr10:43456758-43457107	HepG2	liver:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
12	CEBPB	chr10:43456810-43457012	K562	blood:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
13	CEBPB	chr10:43456879-43457110	Hela-S3	cervix:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
14	CEBPB	chr10:43477134-43477208	K562	blood:	n/a	n/a
15	CEBPB	chr10:43456763-43457109	IMR90	lung:	n/a	chr10:43456929-43456938 chr10:43456928-43456939 chr10:43456927-43456938
16	CEBPB	chr10:43468469-43468786	HepG2	liver:	n/a	chr10:43468625-43468636 chr10:43468624-43468637
17	CEBPB	chr10:43474862-43474980	K562	blood:	n/a	n/a
18	CHD2	chr10:43471209-43471243	HepG2	liver:	n/a	n/a
19	CTCF	chr10:43471160-43471310	HMEC	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
20	CTCF	chr10:43471000-43471150	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr10:43455971-43456059	NHEK	skin:	n/a	n/a
22	CTCF	chr10:43471133-43471394	NHEK	skin:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
23	CTCF	chr10:43455966-43455969	NHEK	skin:	n/a	n/a
24	CTCF	chr10:43471180-43471330	GM12873	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
25	CTCF	chr10:43471200-43471350	GM12873	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
26	CTCF	chr10:43453408-43453514	LNCaP	prostate:	n/a	n/a
27	CTCF	chr10:43471141-43471338	HepG2	liver:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
28	CTCF	chr10:43458880-43459030	K562	blood:	n/a	n/a
29	CTCF	chr10:43471260-43471410	GM12864	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
30	CTCF	chr10:43471180-43471276	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr10:43471180-43471330	A549	lung:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
32	CTCF	chr10:43471160-43471310	GM12871	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
33	CTCF	chr10:43471120-43471270	GM06990	blood:	n/a	n/a
34	CTCF	chr10:43471134-43471359	H1-hESC	embryonic stem cell:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
35	CTCF	chr10:43471156-43471370	Hela-S3	cervix:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
36	CTCF	chr10:43453420-43453570	SAEC	small airway:	n/a	n/a
37	CTCF	chr10:43470740-43470890	NB4	blood:	n/a	n/a
38	CTCF	chr10:43471178-43471330	H1-hESC	embryonic stem cell:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
39	CTCF	chr10:43471063-43471415	MCF-7	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
40	CTCF	chr10:43471221-43471324	Medullo	brain:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
41	CTCF	chr10:43471160-43471310	RPTEC	kidney:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
42	CTCF	chr10:43471160-43471310	GM12870	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
43	CTCF	chr10:43490594-43490694	GM20000	blood:	n/a	n/a
44	CTCF	chr10:43471073-43471350	T-47D	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
45	CTCF	chr10:43471220-43471370	GM12866	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
46	CTCF	chr10:43465520-43465670	GM12866	blood:	n/a	n/a
47	CTCF	chr10:43471180-43471330	GM12865	blood:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
48	CTCF	chr10:43471114-43471407	MCF-7	breast:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
49	CTCF	chr10:43471220-43471370	AG09309	skin:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
50	CTCF	chr10:43453360-43453510	HMEC	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43470988..43471723-chr10:43574194..43574824,2	MCF-7	breast:
2	chr10:43448104..43449836-chr10:43453416..43456002,2	MCF-7	breast:
3	chr10:43465926..43467640-chr10:43469651..43471316,2	K562	blood:
4	chr10:43454969..43457476-chr10:43464603..43467508,2	MCF-7	breast:
5	chr10:43458559..43459070-chr17:7387320..7387822,2	NB4	blood:
6	chr10:43481086..43483555-chr10:43520776..43523098,2	MCF-7	breast:
7	chr10:43474536..43476774-chr10:43520389..43522895,3	MCF-7	breast:
8	chr10:43472744..43475645-chr10:43482853..43485433,2	K562	blood:
9	chr10:43454488..43457151-chr10:43458866..43460532,2	K562	blood:
10	chr10:43472744..43475645-chr10:43482853..43485433,2	K562	blood:
11	chr10:43463562..43467082-chr10:43469575..43473842,3	MCF-7	breast:
12	chr10:43486095..43489357-chr10:43490017..43492485,3	MCF-7	breast:
13	chr10:43450142..43452389-chr10:43455226..43458611,3	K562	blood:
14	chr10:43469169..43471779-chr10:43471792..43473949,2	K562	blood:
15	chr10:43471183..43472148-chr4:106629910..106630418,2	NB4	blood:
16	chr10:43474227..43476529-chr10:43479652..43481353,2	MCF-7	breast:
17	chr10:43454969..43457476-chr10:43464603..43467508,2	MCF-7	breast:
18	chr10:43452048..43454806-chr10:43520323..43522084,2	MCF-7	breast:
19	chr10:43484291..43485932-chr10:43488466..43491187,2	MCF-7	breast:
20	chr10:43423641..43426071-chr10:43452071..43454009,2	MCF-7	breast:
21	chr10:43450408..43453024-chr10:43497080..43499917,2	K562	blood:
22	chr10:43495233..43497382-chr10:43502437..43504369,2	MCF-7	breast:
23	chr10:43454488..43457151-chr10:43458866..43460532,2	K562	blood:
24	chr10:43470043..43470710-chr4:7069530..7070337,2	NB4	blood:
25	chr10:43496061..43498951-chr10:43575386..43576961,2	MCF-7	breast:
26	chr10:43361867..43362389-chr10:43470791..43471531,2	K562	blood:
27	chr10:43450805..43453524-chr10:43455350..43458252,2	MCF-7	breast:
28	chr10:43454448..43456264-chr10:43474294..43477157,2	MCF-7	breast:
29	chr10:43361913..43362690-chr10:43470789..43471679,3	MCF-7	breast:
30	chr10:43465926..43467640-chr10:43469651..43471316,2	K562	blood:
31	chr10:43477135..43480872-chr10:43482623..43485089,4	MCF-7	breast:
32	chr10:43463562..43467082-chr10:43469575..43473842,3	MCF-7	breast:
33	chr10:43494956..43496475-chr10:43498262..43500423,2	K562	blood:
34	chr1:113932116..113933106-chr10:43470154..43470896,2	NB4	blood:
35	chr10:43450805..43453524-chr10:43455350..43458252,2	MCF-7	breast:
36	chr10:43442278..43444933-chr10:43480874..43482921,2	K562	blood:
37	chr10:43482866..43485744-chr10:43490374..43493373,2	K562	blood:
38	chr10:43474227..43476529-chr10:43479652..43481353,2	MCF-7	breast:
39	chr10:43471587..43474099-chr10:43476210..43479281,3	MCF-7	breast:
40	chr10:43484291..43485932-chr10:43488466..43491187,2	MCF-7	breast:
41	chr10:43471160..43472154-chr11:102217419..102218246,2	NB4	blood:
42	chr10:43469610..43472857-chr10:43520371..43524809,5	MCF-7	breast:
43	chr10:43487519..43490099-chr10:43491819..43493663,2	MCF-7	breast:
44	chr10:43450408..43453024-chr10:43497080..43499917,2	K562	blood:
45	chr10:43467866..43472352-chr10:43571131..43575180,5	MCF-7	breast:
46	chr10:43494122..43496846-chr10:43520768..43523139,2	MCF-7	breast:
47	chr10:43495233..43497382-chr10:43502437..43504369,2	MCF-7	breast:
48	chr10:43472048..43472812-chr11:819441..820070,2	NB4	blood:
49	chr10:43477135..43480872-chr10:43482623..43485089,4	MCF-7	breast:
50	chr10:43469169..43471779-chr10:43471792..43473949,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RET-2	chr10:43482124-43482459	NONHSAT012938
2	lnc-RASGEF1A-1	chr10:43474465-43474547	XLOC_008790
3	lnc-RET-3	chr10:43487172-43487532	ucscGeneNc_uc001jba_2
4	lnc-RET-3	chr10:43487762-43487899	ucscGeneNc_uc001jba_2
5	lnc-RASGEF1A-1	chr10:43475731-43476007	XLOC_008790
6	lnc-RET-2	chr10:43481122-43481247	NONHSAT012938
7	lnc-RET-3	chr10:43489288-43490153	ucscGeneNc_uc001jba_2
8	lnc-RET-3	chr10:43486575-43486975	ucscGeneNc_uc001jba_2
9	lnc-RASGEF1A-1	chr10:43476816-43476955	XLOC_008790

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5100	chr10:43493078-43493099	MIMAT0022259

Variant related genes	Relation type
MIR5100	TF binding region
ENSG00000229630	TF binding region
ENSG00000110330	chromatin interactions
ENSG00000109519	chromatin interactions
ENSG00000138780	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000229630	chromatin interactions
ENSG00000136059	chromatin interactions
ENSG00000077458	chromatin interactions
ENSG00000263795	chromatin interactions
ENSG00000166037	chromatin interactions
ENSG00000138785	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000181222	chromatin interactions

Extended variants
information (count: 2257 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2257 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2506034	chr10:43452436-43452437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191743820	chr10:43452461-43452462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532160564	chr10:43452524-43452525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375366860	chr10:43452538-43452539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs202145180	chr10:43452586-43452587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141981702	chr10:43452620-43452621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183580098	chr10:43452630-43452631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115807894	chr10:43452666-43452667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188727666	chr10:43452690-43452691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192384707	chr10:43452692-43452693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184724243	chr10:43452700-43452701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559077311	chr10:43452760-43452761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528036684	chr10:43452775-43452776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529481576	chr10:43452837-43452838	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs571082681	chr10:43452927-43452928	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs72779303	chr10:43452972-43452973	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs556622444	chr10:43452983-43452984	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs575039536	chr10:43452995-43452996	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs578221695	chr10:43453042-43453043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542263888	chr10:43453067-43453068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554118552	chr10:43453107-43453108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540925223	chr10:43453114-43453115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186512764	chr10:43453217-43453218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74135430	chr10:43453277-43453278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12414487	chr10:43453310-43453311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150501008	chr10:43453339-43453340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58288950	chr10:43453341-43453342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200330114	chr10:43453344-43453345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397739642	chr10:43453345-43453346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555711527	chr10:43453346-43453347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138748607	chr10:43453347-43453348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11239844	chr10:43453365-43453366	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs184881335	chr10:43453367-43453368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189720391	chr10:43453369-43453370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192940489	chr10:43453396-43453397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542187664	chr10:43453397-43453398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145718236	chr10:43453463-43453464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529972245	chr10:43453565-43453566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562269841	chr10:43453597-43453598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77841484	chr10:43453615-43453616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138733035	chr10:43453625-43453626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551199536	chr10:43453702-43453703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370402439	chr10:43453710-43453711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571105232	chr10:43453740-43453741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115159410	chr10:43453757-43453758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185049446	chr10:43453830-43453831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570074799	chr10:43453844-43453845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189075618	chr10:43453847-43453848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181798398	chr10:43453868-43453869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141297632	chr10:43453872-43453873	Enhancers 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:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43447600-43455800	Weak transcription	Left Ventricle	heart
2	chr10:43448600-43456200	Weak transcription	Right Ventricle	heart
3	chr10:43452800-43453000	ZNF genes & repeats	HSMMtube	muscle
4	chr10:43453000-43455800	Weak transcription	HSMMtube	muscle
5	chr10:43453400-43459200	Enhancers	Fetal Muscle Leg	muscle
6	chr10:43454400-43455000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr10:43454600-43454800	Weak transcription	Psoas Muscle	Psoas
8	chr10:43454800-43455000	Enhancers	Psoas Muscle	Psoas
9	chr10:43454800-43458600	Enhancers	Spleen	Spleen
10	chr10:43454800-43458800	Enhancers	Fetal Muscle Trunk	muscle
11	chr10:43455000-43455800	Weak transcription	Psoas Muscle	Psoas
12	chr10:43455200-43457600	Enhancers	HMEC	breast
13	chr10:43455400-43456600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr10:43455400-43457400	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr10:43455400-43457600	Enhancers	NHEK	skin
16	chr10:43455600-43456800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr10:43455600-43458000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr10:43455800-43456400	Enhancers	Muscle Satellite Cultured Cells	--
19	chr10:43455800-43456400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr10:43455800-43456600	Enhancers	HSMMtube	muscle
21	chr10:43455800-43457000	Enhancers	HSMM	muscle
22	chr10:43455800-43458000	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr10:43455800-43458400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr10:43455800-43458400	Enhancers	Placenta	Placenta
25	chr10:43455800-43458600	Enhancers	Left Ventricle	heart
26	chr10:43455800-43458600	Enhancers	Psoas Muscle	Psoas
27	chr10:43455800-43458600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
28	chr10:43455800-43460200	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr10:43456000-43456400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr10:43456000-43458200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr10:43456000-43458600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr10:43456000-43458600	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr10:43456200-43456600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr10:43456200-43457800	Enhancers	Right Atrium	heart
35	chr10:43456200-43458400	Enhancers	Right Ventricle	heart
36	chr10:43456400-43456600	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr10:43456400-43457000	Enhancers	Pancreas	Pancrea
38	chr10:43456400-43457400	Enhancers	Fetal Stomach	stomach
39	chr10:43456400-43457600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr10:43456400-43459400	Enhancers	Adipose Nuclei	Adipose
41	chr10:43456600-43457000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr10:43456600-43457000	Weak transcription	HSMMtube	muscle
43	chr10:43456600-43461800	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr10:43456800-43458000	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr10:43456800-43459000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr10:43457000-43457200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr10:43457000-43457400	Enhancers	HSMMtube	muscle
48	chr10:43457200-43458200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr10:43457200-43458200	Enhancers	Fetal Lung	lung
50	chr10:43457400-43457600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle

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