Variant report

Variant	nsv907027
Chromosome Location	chr16:82830121-82871350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:117)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:117 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr16:82835024-82835307	GM12878	blood:	n/a	n/a
2	BATF	chr16:82834943-82835371	GM12878	blood:	n/a	n/a
3	CEBPB	chr16:82866492-82866844	IMR90	lung:	n/a	n/a
4	CEBPB	chr16:82852019-82852166	A549	lung:	n/a	n/a
5	CTCF	chr16:82867920-82868070	HPF	lung:	n/a	chr16:82867941-82867954
6	CTCF	chr16:82857960-82858110	HCM	heart:	n/a	n/a
7	CTCF	chr16:82858100-82858250	GM12871	blood:	n/a	n/a
8	CTCF	chr16:82835080-82835230	HBMEC	blood vessel:	n/a	n/a
9	CTCF	chr16:82858127-82858143	Spleen_OC	spleen:	n/a	n/a
10	CTCF	chr16:82867860-82868010	HPAF	blood vessel:	n/a	chr16:82867941-82867954
11	CTCF	chr16:82835040-82835190	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr16:82858137-82858240	GM13976	blood:	n/a	n/a
13	CTCF	chr16:82858000-82858150	RPTEC	kidney:	n/a	n/a
14	CTCF	chr16:82835120-82835270	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr16:82867800-82867950	AG10803	skin:	n/a	n/a
16	CTCF	chr16:82831920-82832070	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr16:82858171-82858188	GM13977	blood:	n/a	n/a
18	CTCF	chr16:82835000-82835150	HMF	breast:	n/a	n/a
19	CTCF	chr16:82867860-82868010	AG04450	lung:	n/a	chr16:82867941-82867954
20	CTCF	chr16:82858115-82858180	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr16:82867820-82867970	HCM	heart:	n/a	chr16:82867941-82867954
22	CTCF	chr16:82867760-82867910	HVMF	connective:	n/a	n/a
23	CTCF	chr16:82835100-82835250	HCFaa	heart:	n/a	n/a
24	CTCF	chr16:82835100-82835250	HMF	breast:	n/a	n/a
25	CTCF	chr16:82858003-82858292	GM12878	blood:	n/a	n/a
26	CTCF	chr16:82867856-82867995	SK-N-SH_RA	brain:	n/a	chr16:82867941-82867954
27	CTCF	chr16:82867800-82867950	HPF	lung:	n/a	n/a
28	CTCF	chr16:82835120-82835270	AG04450	lung:	n/a	n/a
29	CTCF	chr16:82858000-82858150	HCFaa	heart:	n/a	n/a
30	CTCF	chr16:82867860-82868010	AoAF	blood vessel:	n/a	chr16:82867941-82867954
31	CTCF	chr16:82867860-82868010	AG04449	skin:	n/a	chr16:82867941-82867954
32	CTCF	chr16:82867880-82868030	AG04450	lung:	n/a	chr16:82867941-82867954
33	CTCF	chr16:82867880-82868030	HCM	heart:	n/a	chr16:82867941-82867954
34	CTCF	chr16:82858060-82858210	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr16:82847900-82848050	GM12875	blood:	n/a	n/a
36	CTCF	chr16:82858106-82858212	K562	blood:	n/a	n/a
37	CTCF	chr16:82858080-82858230	GM12871	blood:	n/a	n/a
38	CTCF	chr16:82858080-82858230	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr16:82867900-82868050	HAc	cerebellar:	n/a	chr16:82867941-82867954
40	CTCF	chr16:82835100-82835250	AG09309	skin:	n/a	n/a
41	CTCF	chr16:82867940-82868090	HBMEC	blood vessel:	n/a	chr16:82867941-82867954
42	CTCF	chr16:82858144-82858151	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr16:82858020-82858170	GM12873	blood:	n/a	n/a
44	CTCF	chr16:82857960-82858230	RPTEC	kidney:	n/a	n/a
45	CTCF	chr16:82858094-82858196	GM12878	blood:	n/a	n/a
46	CTCF	chr16:82867860-82868010	HBMEC	blood vessel:	n/a	chr16:82867941-82867954
47	CTCF	chr16:82858100-82858250	HMF	breast:	n/a	n/a
48	CTCF	chr16:82867880-82868030	AG04449	skin:	n/a	chr16:82867941-82867954
49	EBF1	chr16:82849099-82849258	GM12878	blood:	n/a	chr16:82849186-82849197 chr16:82849186-82849199 chr16:82849188-82849197
50	FOS	chr16:82866559-82866759	MCF10A-Er-Src	breast:	n/a	chr16:82866664-82866674 chr16:82866665-82866673 chr16:82866664-82866674

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:82868296-82868346	PANC-1	pancreas:	n/a
2	chr16:82868296-82868346	NHBE	bronchial:	n/a
3	chr16:82868296-82868346	CMK	blood:	n/a
4	chr16:82868296-82868346	SKMC	muscle:	n/a
5	chr16:82868296-82868346	HRE	kidney:	n/a
6	chr16:82868296-82868346	HIPEpiC	eye:	n/a
7	chr16:82868296-82868346	HAEpiC	amniotic membrane:	n/a
8	chr16:82868296-82868346	HCM	heart:	n/a
9	chr16:82868296-82868346	MCF-7	breast:	n/a
10	chr16:82868296-82868346	K562	blood:	n/a
11	chr16:82868296-82868346	PFSK-1	brain:	n/a
12	chr16:82868296-82868346	HL-60	blood:	n/a
13	chr16:82868296-82868346	GM06990	blood:	n/a
14	chr16:82868296-82868346	AoSMC	blood vessel:	n/a
15	chr16:82868296-82868346	RPTEC	kidney:	n/a
16	chr16:82868296-82868346	ovcar-3	ovarian:	n/a
17	chr16:82868296-82868346	AG10803	skin:	n/a
18	chr16:82868296-82868346	Hela-S3	cervix:	n/a
19	chr16:82868296-82868346	HNPCEpiC	eye:	n/a
20	chr16:82868296-82868346	PrEC	prostate:	n/a
21	chr16:82868296-82868346	SK-N-MC	brain:	n/a
22	chr16:82868296-82868346	HepG2	liver:	n/a
23	chr16:82868296-82868346	HEK293	kidney:	embryo
24	chr16:82868296-82868346	BE2_C	brain:	n/a
25	chr16:82868296-82868346	AG09319	gingival:	n/a
26	chr16:82868296-82868346	AG09309	skin:	n/a
27	chr16:82868296-82868346	A549	lung:	n/a
28	chr16:82868296-82868346	BJ	skin:	n/a
29	chr16:82868296-82868346	HPAEpiC	pulmonary alveolar:	n/a
30	chr16:82868296-82868346	Hepatocyte	liver:	n/a
31	chr16:82868296-82868346	HRPEpiC	eye:	n/a
32	chr16:82868296-82868346	HCPEpiC	choroid plexus:	n/a
33	chr16:82868296-82868346	GM12878	blood:	n/a
34	chr16:82868296-82868346	ECC-1	luminal epithelium:	n/a
35	chr16:82868296-82868346	Jurkat	blood:	n/a
36	chr16:82868296-82868346	NHDF-neo	bronchial:	n/a
37	chr16:82868296-82868346	SK-N-SH	brain:	n/a
38	chr16:82868296-82868346	U87	brain:	n/a
39	chr16:82868296-82868346	H1-hESC	embryonic stem cell:	embryo
40	chr16:82868296-82868346	NT2-D1	testis:	n/a
41	chr16:82868296-82868346	LNCaP	prostate:	n/a
42	chr16:82868296-82868346	AG04449	skin:	fetal
43	chr16:82868296-82868346	Caco-2	colon:	n/a
44	chr16:82868296-82868346	AG04450	lung:	fetal
45	chr16:82868296-82868346	HCF	heart:	n/a
46	chr16:82868296-82868346	HCT-116	colon:	n/a
47	chr16:82868296-82868346	HEEpiC	esophagus:	n/a
48	chr16:82868296-82868346	T-47D	breast:	n/a
49	chr16:82868296-82868346	SAEC	small airway:	n/a
50	chr16:82868296-82868346	HRCEpiC	kidney:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:82851793..82853515-chr16:82855171..82856749,2	K562	blood:
2	chr16:82851793..82853515-chr16:82855171..82856749,2	K562	blood:
3	chr16:82862726..82865339-chr16:82908462..82910658,2	MCF-7	breast:
4	chr16:82838532..82841265-chr16:82844045..82845845,2	MCF-7	breast:
5	chr16:82838532..82841265-chr16:82844045..82845845,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSD17B2-2	chr16:82856817-82860308	ENSG00000260862.1
2	lnc-HSD17B2-2	chr16:82862870-82863243	ENSG00000260862.1

No data

Variant related genes	Relation type
ENSG00000221395	TF binding region
ENSG00000221395	CpG island

Extended variants
information (count: 2643 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2643 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11644588	chr16:82830121-82830122	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536496247	chr16:82830135-82830136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554748109	chr16:82830141-82830142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576191221	chr16:82830181-82830182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543527905	chr16:82830191-82830192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139274362	chr16:82830195-82830196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143173017	chr16:82830219-82830220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147488669	chr16:82830224-82830225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559433471	chr16:82830238-82830239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184918435	chr16:82830239-82830240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77407312	chr16:82830269-82830270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563487797	chr16:82830275-82830276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532730187	chr16:82830292-82830293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530696301	chr16:82830310-82830311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10514567	chr16:82830349-82830350	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs570511736	chr16:82830359-82830360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189722835	chr16:82830360-82830361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534361418	chr16:82830393-82830394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546573748	chr16:82830405-82830406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567672501	chr16:82830413-82830414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376800795	chr16:82830444-82830445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182513158	chr16:82830450-82830451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185627404	chr16:82830477-82830478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62036792	chr16:82830479-82830480	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531894019	chr16:82830484-82830485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537228583	chr16:82830486-82830487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558823226	chr16:82830487-82830488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577262682	chr16:82830496-82830497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555620725	chr16:82830510-82830511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541117891	chr16:82830513-82830514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190428549	chr16:82830546-82830547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78562558	chr16:82830549-82830550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542166624	chr16:82830560-82830561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75312871	chr16:82830572-82830573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568531212	chr16:82830585-82830586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545969367	chr16:82830599-82830600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183539420	chr16:82830606-82830607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528194629	chr16:82830623-82830624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546340035	chr16:82830634-82830635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149564367	chr16:82830653-82830654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188735951	chr16:82830663-82830664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144255383	chr16:82830681-82830682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570002574	chr16:82830684-82830685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193026829	chr16:82830698-82830699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4783281	chr16:82830719-82830720	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs570915066	chr16:82830751-82830752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553460251	chr16:82830753-82830754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148716321	chr16:82830762-82830763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553475190	chr16:82830767-82830768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574914256	chr16:82830768-82830769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Non-small cell lung cancer	21829676	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16461572	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Alveolar capillary dysplasia	19500772	CNVD
VACTERL syndrome	21315191	CNVD
T-cell lymphomas	19863542	CNVD
Developmental delay	19490664	CNVD
Neuroblastoma	18923191	CNVD
Adrenocortical carcinoma	18281524	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82810600-82834800	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr16:82815800-82834600	Weak transcription	HUVEC	blood vessel
3	chr16:82817200-82838800	Weak transcription	Psoas Muscle	Psoas
4	chr16:82818400-82839600	Weak transcription	Aorta	Aorta
5	chr16:82819600-82833800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr16:82820200-82838600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr16:82822600-82833800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr16:82822800-82839000	Weak transcription	Left Ventricle	heart
9	chr16:82823200-82832200	Weak transcription	HMEC	breast
10	chr16:82823600-82858000	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr16:82825800-82833000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr16:82827600-82838200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr16:82827800-82834000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr16:82828600-82832400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr16:82828600-82833200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr16:82828600-82833400	Strong transcription	HSMM	muscle
17	chr16:82829000-82831200	Weak transcription	Right Ventricle	heart
18	chr16:82829000-82832200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr16:82829400-82856600	Weak transcription	NHEK	skin
20	chr16:82829600-82838600	Weak transcription	HSMMtube	muscle
21	chr16:82829800-82830200	Strong transcription	Fetal Muscle Leg	muscle
22	chr16:82830200-82833200	Weak transcription	Fetal Muscle Leg	muscle
23	chr16:82831200-82832400	Enhancers	Fetal Heart	heart
24	chr16:82832200-82833000	Strong transcription	HMEC	breast
25	chr16:82832200-82833600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr16:82832400-82834400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr16:82833000-82835800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr16:82833000-82873600	Weak transcription	HMEC	breast
29	chr16:82833200-82840200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr16:82833400-82835000	Weak transcription	HSMM	muscle
31	chr16:82833600-82848600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr16:82834000-82834200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr16:82834400-82836000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr16:82834600-82835000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr16:82834600-82835200	Enhancers	NHDF-Ad	bronchial
36	chr16:82834600-82835600	Enhancers	HUVEC	blood vessel
37	chr16:82834800-82835200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr16:82834800-82835200	Enhancers	NH-A	brain
39	chr16:82834800-82835400	Enhancers	Osteobl	bone
40	chr16:82834800-82836000	Enhancers	GM12878-XiMat	blood
41	chr16:82835000-82836600	Strong transcription	HSMM	muscle
42	chr16:82835400-82839200	Weak transcription	Osteobl	bone
43	chr16:82835600-82845800	Weak transcription	HUVEC	blood vessel
44	chr16:82835800-82836400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr16:82836000-82841200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr16:82836400-82841800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr16:82836600-82848800	Weak transcription	HSMM	muscle
48	chr16:82838600-82838800	Enhancers	HSMMtube	muscle
49	chr16:82838600-82839400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr16:82838800-82839200	Weak transcription	HSMMtube	muscle

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