Variant report

Variant	nsv907003
Chromosome Location	chr16:80919668-80951145
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:122)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:80948054-80948715	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:80944278-80944659	HepG2	liver:	n/a	n/a
3	ATF1	chr16:80944704-80944828	K562	blood:	n/a	n/a
4	BACH1	chr16:80927684-80927727	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr16:80923667-80923938	GM12878	blood:	n/a	n/a
6	BHLHE40	chr16:80948237-80948809	HepG2	liver:	n/a	n/a
7	BHLHE40	chr16:80924003-80924197	GM12878	blood:	n/a	n/a
8	BRCA1	chr16:80926404-80926634	GM12878	blood:	n/a	n/a
9	CEBPB	chr16:80926667-80926947	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr16:80927983-80928280	HepG2	liver:	n/a	n/a
11	CEBPB	chr16:80926597-80926928	K562	blood:	n/a	n/a
12	CEBPB	chr16:80924006-80924206	HepG2	liver:	n/a	n/a
13	CEBPB	chr16:80923976-80924189	A549	lung:	n/a	n/a
14	CEBPB	chr16:80923994-80924200	K562	blood:	n/a	n/a
15	CEBPB	chr16:80948239-80948638	HepG2	liver:	n/a	n/a
16	CEBPB	chr16:80926611-80926963	HepG2	liver:	n/a	n/a
17	CEBPB	chr16:80948177-80948731	HepG2	liver:	n/a	n/a
18	CEBPB	chr16:80948252-80948696	HepG2	liver:	n/a	n/a
19	CEBPB	chr16:80936662-80936967	HepG2	liver:	n/a	chr16:80936816-80936827 chr16:80936815-80936828
20	CEBPB	chr16:80926730-80926848	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr16:80948359-80948578	HepG2	liver:	n/a	n/a
22	CEBPB	chr16:80923968-80924141	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr16:80926682-80926923	A549	lung:	n/a	n/a
24	CHD2	chr16:80926360-80926747	K562	blood:	n/a	n/a
25	CHD2	chr16:80926359-80926676	GM12878	blood:	n/a	n/a
26	CHD2	chr16:80934284-80934373	HepG2	liver:	n/a	n/a
27	CTCF	chr16:80934320-80934470	AG09319	gingival:	n/a	n/a
28	CTCF	chr16:80934300-80934450	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr16:80934420-80934570	HAc	cerebellar:	n/a	n/a
30	CTCF	chr16:80934400-80934550	NHLF	lung:	n/a	n/a
31	CTCF	chr16:80936580-80936730	HepG2	liver:	n/a	chr16:80936671-80936684 chr16:80936636-80936649
32	CTCF	chr16:80934260-80934410	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr16:80934320-80934470	AG09309	skin:	n/a	n/a
34	CTCF	chr16:80934280-80934430	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr16:80930040-80930190	Hela-S3	cervix:	n/a	n/a
36	E2F4	chr16:80934258-80934432	MCF10A-Er-Src	breast:	n/a	n/a
37	EBF1	chr16:80925984-80926024	GM12878	blood:	n/a	n/a
38	ELF1	chr16:80948578-80948905	K562	blood:	n/a	chr16:80948735-80948748
39	ELF1	chr16:80948266-80948970	HepG2	liver:	n/a	chr16:80948735-80948748
40	ELF1	chr16:80948348-80948909	HepG2	liver:	n/a	chr16:80948735-80948748
41	EP300	chr16:80944276-80944755	HepG2	liver:	n/a	n/a
42	EP300	chr16:80943645-80944033	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr16:80934082-80934719	T-47D	breast:	n/a	chr16:80934444-80934453
44	EP300	chr16:80923788-80924028	GM12878	blood:	n/a	n/a
45	EP300	chr16:80948001-80948868	HepG2	liver:	n/a	n/a
46	EP300	chr16:80925510-80925513	GM12878	blood:	n/a	n/a
47	EP300	chr16:80934031-80934769	T-47D	breast:	n/a	chr16:80934444-80934453
48	EP300	chr16:80944304-80944635	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr16:80923664-80923869	GM12878	blood:	n/a	n/a
50	EP300	chr16:80948264-80948736	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:80934340-80934390	GM06990	blood:	n/a
2	chr16:80926783-80926833	Jurkat	blood:	n/a
3	chr16:80926783-80926833	IMR90	lung:	fetal
4	chr16:80926783-80926833	PrEC	prostate:	n/a
5	chr16:80926783-80926833	GM19239	blood:	n/a
6	chr16:80926783-80926833	AG10803	skin:	n/a
7	chr16:80926783-80926833	GM12891	blood:	n/a
8	chr16:80926783-80926833	ProgFib	skin:	n/a
9	chr16:80934340-80934390	ProgFib	skin:	n/a
10	chr16:80926783-80926833	SK-N-SH_RA	brain:	n/a
11	chr16:80934340-80934390	HNPCEpiC	eye:	n/a
12	chr16:80934340-80934390	SAEC	small airway:	n/a
13	chr16:80926783-80926833	NH-A	brain:	n/a
14	chr16:80934340-80934390	SK-N-SH_RA	brain:	n/a
15	chr16:80926783-80926833	GM12878	blood:	n/a
16	chr16:80934340-80934390	HEK293	kidney:	embryo
17	chr16:80934340-80934390	IMR90	lung:	fetal
18	chr16:80934340-80934390	Hepatocyte	liver:	n/a
19	chr16:80926783-80926833	RPTEC	kidney:	n/a
20	chr16:80934340-80934390	HCT-116	colon:	n/a
21	chr16:80934340-80934390	Jurkat	blood:	n/a
22	chr16:80934340-80934390	HUVEC	blood vessel:	n/a
23	chr16:80934340-80934390	BJ	skin:	n/a
24	chr16:80934340-80934390	NB4	blood:	n/a
25	chr16:80926783-80926833	HPAEpiC	pulmonary alveolar:	n/a
26	chr16:80926783-80926833	AG04449	skin:	fetal
27	chr16:80926783-80926833	U87	brain:	n/a
28	chr16:80934340-80934390	K562	blood:	n/a
29	chr16:80926783-80926833	HUVEC	blood vessel:	n/a
30	chr16:80926783-80926833	HRCEpiC	kidney:	n/a
31	chr16:80926783-80926833	HAEpiC	amniotic membrane:	n/a
32	chr16:80934340-80934390	MCF-7	breast:	n/a
33	chr16:80926783-80926833	NB4	blood:	n/a
34	chr16:80926783-80926833	BJ	skin:	n/a
35	chr16:80934340-80934390	ovcar-3	ovarian:	n/a
36	chr16:80926783-80926833	BE2_C	brain:	n/a
37	chr16:80934340-80934390	HRE	kidney:	n/a
38	chr16:80926783-80926833	HEK293	kidney:	embryo
39	chr16:80926783-80926833	H1-hESC	embryonic stem cell:	embryo
40	chr16:80926783-80926833	AG09319	gingival:	n/a
41	chr16:80926783-80926833	K562	blood:	n/a
42	chr16:80926783-80926833	NHDF-neo	bronchial:	n/a
43	chr16:80934340-80934390	HPAEpiC	pulmonary alveolar:	n/a
44	chr16:80934340-80934390	A549	lung:	n/a
45	chr16:80934340-80934390	AG09309	skin:	n/a
46	chr16:80926783-80926833	SK-N-SH	brain:	n/a
47	chr16:80926783-80926833	HRPEpiC	eye:	n/a
48	chr16:80934340-80934390	AG09319	gingival:	n/a
49	chr16:80934340-80934390	Caco-2	colon:	n/a
50	chr16:80926783-80926833	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:80915029..80919258-chr16:80920866..80924672,3	K562	blood:
2	chr16:80950553..80953339-chr16:80965421..80967122,2	MCF-7	breast:
3	chr16:80943433..80946323-chr16:80947532..80951132,3	K562	blood:
4	chr16:80886274..80886849-chr16:80933809..80934549,2	MCF-7	breast:
5	chr16:80943433..80946323-chr16:80947532..80951132,3	K562	blood:
6	chr16:80934136..80935962-chr16:80936388..80938023,2	MCF-7	breast:
7	chr16:80921858..80922727-chr8:73759123..73759980,2	MCF-7	breast:
8	chr15:52970973..52971687-chr16:80951115..80952002,2	MCF-7	breast:
9	chr16:80930799..80932496-chr16:80932538..80934325,2	MCF-7	breast:
10	chr16:80909329..80911458-chr16:80945639..80947612,2	MCF-7	breast:
11	chr16:80915855..80918069-chr16:80933257..80936088,3	MCF-7	breast:
12	chr16:80934136..80935962-chr16:80936388..80938023,2	MCF-7	breast:
13	chr16:80930799..80932496-chr16:80932538..80934325,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDYL2-4	chr16:80926402-80926457	ENSG00000260896.1
2	lnc-CDYL2-4	chr16:80926402-80926492	ENSG00000260896.1

No data

Variant related genes	Relation type
ENSG00000260896	TF binding region
ENSG00000260896	CpG island
ENSG00000047346	chromatin interactions

Extended variants
information (count: 1640 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9925502	chr16:80919668-80919669	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554042181	chr16:80919677-80919678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181591838	chr16:80919687-80919688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373592686	chr16:80919688-80919689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542897295	chr16:80919690-80919691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554870705	chr16:80919704-80919705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575627848	chr16:80919709-80919710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs74028817	chr16:80919734-80919735	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs2549864	chr16:80919772-80919773	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs72811825	chr16:80919788-80919789	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs141110767	chr16:80919840-80919841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555261082	chr16:80919921-80919922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559267062	chr16:80919928-80919929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74028818	chr16:80919932-80919933	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs2549747	chr16:80919943-80919944	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs2549746	chr16:80919985-80919986	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs143728903	chr16:80920031-80920032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2580302	chr16:80920045-80920046	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs549858451	chr16:80920048-80920049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2549745	chr16:80920076-80920077	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs538721968	chr16:80920094-80920095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111697618	chr16:80920125-80920126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369490014	chr16:80920138-80920139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2549744	chr16:80920167-80920168	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs536494353	chr16:80920182-80920183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371869641	chr16:80920211-80920212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150483058	chr16:80920232-80920233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186313955	chr16:80920235-80920236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35723088	chr16:80920245-80920246	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs543534539	chr16:80920248-80920249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191153816	chr16:80920266-80920267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558234676	chr16:80920305-80920306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546903455	chr16:80920319-80920320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs72414387	chr16:80920332-80920333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576807505	chr16:80920354-80920355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs151146296	chr16:80920369-80920370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113965256	chr16:80920372-80920373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182176302	chr16:80920388-80920389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28620803	chr16:80920447-80920448	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs2580303	chr16:80920448-80920449	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs186673330	chr16:80920490-80920491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531965746	chr16:80920534-80920535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530795877	chr16:80920552-80920553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552458919	chr16:80920561-80920562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565116740	chr16:80920563-80920564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554256139	chr16:80920564-80920565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs199863977	chr16:80920572-80920573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375956654	chr16:80920577-80920578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200980066	chr16:80920578-80920579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs200685420	chr16:80920595-80920596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80917000-80920000	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr16:80917400-80919800	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr16:80918200-80920800	Weak transcription	HepG2	liver
4	chr16:80918400-80921000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr16:80918800-80919800	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr16:80918800-80920600	Weak transcription	Fetal Intestine Large	intestine
7	chr16:80919000-80920400	Weak transcription	Fetal Intestine Small	intestine
8	chr16:80919600-80921000	Weak transcription	Gastric	stomach
9	chr16:80919800-80920800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr16:80920000-80920400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr16:80920400-80921000	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr16:80920400-80921600	Enhancers	Fetal Intestine Small	intestine
13	chr16:80920600-80921600	Enhancers	Fetal Intestine Large	intestine
14	chr16:80920800-80921000	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr16:80920800-80921600	Enhancers	HepG2	liver
16	chr16:80921000-80921200	Enhancers	Duodenum Mucosa	Duodenum
17	chr16:80921000-80921400	Enhancers	Gastric	stomach
18	chr16:80921000-80921400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr16:80921000-80921400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
20	chr16:80921200-80921400	Flanking Active TSS	Duodenum Mucosa	Duodenum
21	chr16:80921400-80921600	Active TSS	Rectal Mucosa Donor 29	rectum
22	chr16:80921400-80921600	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr16:80921400-80921800	Enhancers	Duodenum Mucosa	Duodenum
24	chr16:80921800-80922800	Weak transcription	Duodenum Mucosa	Duodenum
25	chr16:80922800-80923800	Enhancers	Duodenum Mucosa	Duodenum
26	chr16:80922800-80924200	Enhancers	Small Intestine	intestine
27	chr16:80926000-80926200	Active TSS	GM12878-XiMat	blood
28	chr16:80926000-80927000	Enhancers	Primary B cells from peripheral blood	blood
29	chr16:80926200-80926400	Flanking Active TSS	GM12878-XiMat	blood
30	chr16:80926400-80926800	Active TSS	GM12878-XiMat	blood
31	chr16:80926600-80934600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr16:80926800-80927000	Enhancers	GM12878-XiMat	blood
33	chr16:80927400-80929400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr16:80927600-80928600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr16:80927800-80928200	Enhancers	HepG2	liver
36	chr16:80927800-80928600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr16:80927800-80928800	Enhancers	Fetal Intestine Large	intestine
38	chr16:80928200-80928600	Enhancers	Osteobl	bone
39	chr16:80928400-80928600	Enhancers	Ovary	ovary
40	chr16:80928400-80929400	Enhancers	Fetal Muscle Leg	muscle
41	chr16:80928600-80933200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr16:80928600-80933400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr16:80928600-80933400	Weak transcription	Osteobl	bone
44	chr16:80929400-80930800	Weak transcription	Fetal Muscle Leg	muscle
45	chr16:80930600-80931000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr16:80930600-80931800	Enhancers	Fetal Muscle Trunk	muscle
47	chr16:80930800-80931000	Enhancers	Fetal Muscle Leg	muscle
48	chr16:80930800-80931000	Enhancers	Right Atrium	heart
49	chr16:80931000-80931400	Weak transcription	Fetal Muscle Leg	muscle
50	chr16:80931000-80934200	Weak transcription	Right Atrium	heart

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