Variant report

Variant	nsv457539
Chromosome Location	chr16:76777664-77081676
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1218)
CpG islands
(count:0)
Chromatin interactive
region (count:30)
LncRNA
region (count:7)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1218 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:76913373-76913653	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:76934165-76934485	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:76980885-76981085	K562	blood:	n/a	n/a
4	ATF1	chr16:76789952-76789998	K562	blood:	n/a	n/a
5	ATF2	chr16:77010103-77010377	GM12878	blood:	n/a	n/a
6	ATF2	chr16:76839037-76839302	GM12878	blood:	n/a	n/a
7	ATF3	chr16:76980721-76981225	A549	lung:	n/a	n/a
8	ATF3	chr16:76980774-76981124	K562	blood:	n/a	n/a
9	ATF3	chr16:77003970-77004466	A549	lung:	n/a	n/a
10	ATF3	chr16:76980737-76981284	A549	lung:	n/a	n/a
11	BACH1	chr16:76980722-76981230	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr16:77057336-77057341	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr16:76980807-76981126	K562	blood:	n/a	n/a
14	BATF	chr16:76850433-76850727	GM12878	blood:	n/a	chr16:76850562-76850573
15	BATF	chr16:76966506-76966724	GM12878	blood:	n/a	chr16:76966611-76966622 chr16:76966612-76966622
16	BATF	chr16:76966490-76966773	GM12878	blood:	n/a	chr16:76966611-76966622 chr16:76966612-76966622
17	BATF	chr16:76856386-76856604	GM12878	blood:	n/a	n/a
18	BATF	chr16:76850471-76850665	GM12878	blood:	n/a	chr16:76850562-76850573
19	BATF	chr16:76856327-76856649	GM12878	blood:	n/a	n/a
20	BATF	chr16:76980831-76981097	GM12878	blood:	n/a	chr16:76980965-76980976
21	BATF	chr16:76980823-76981049	GM12878	blood:	n/a	chr16:76980965-76980976
22	BATF	chr16:76838952-76839361	GM12878	blood:	n/a	n/a
23	BATF	chr16:76838975-76839411	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:77010106-77010349	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:76839121-76839299	GM12878	blood:	n/a	chr16:76839215-76839224 chr16:76839226-76839235
26	BCL11A	chr16:76839015-76839347	GM12878	blood:	n/a	chr16:76839215-76839224 chr16:76839226-76839235
27	BCL3	chr16:76980667-76981333	A549	lung:	n/a	n/a
28	BHLHE40	chr16:76980800-76981182	K562	blood:	n/a	n/a
29	BHLHE40	chr16:76981970-76981973	HepG2	liver:	n/a	n/a
30	BHLHE40	chr16:76937293-76937310	HepG2	liver:	n/a	n/a
31	BHLHE40	chr16:76968723-76968754	HepG2	liver:	n/a	n/a
32	CCNT2	chr16:76980827-76981168	K562	blood:	n/a	n/a
33	CEBPB	chr16:76887158-76887345	HepG2	liver:	n/a	n/a
34	CEBPB	chr16:76857050-76857179	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr16:76946832-76947044	HepG2	liver:	n/a	chr16:76946917-76946930 chr16:76946917-76946930 chr16:76946918-76946929
36	CEBPB	chr16:76811841-76811942	HepG2	liver:	n/a	n/a
37	CEBPB	chr16:77039634-77039893	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:76920186-76920327	H1-hESC	embryonic stem cell:	n/a	chr16:76920306-76920323
39	CEBPB	chr16:76990756-76991050	A549	lung:	n/a	n/a
40	CEBPB	chr16:76857365-76857551	HepG2	liver:	n/a	n/a
41	CEBPB	chr16:76952420-76952678	A549	lung:	n/a	n/a
42	CEBPB	chr16:76782214-76782511	A549	lung:	n/a	chr16:76782369-76782380
43	CEBPB	chr16:76944800-76945363	A549	lung:	n/a	n/a
44	CEBPB	chr16:76782202-76782512	HepG2	liver:	n/a	chr16:76782369-76782380
45	CEBPB	chr16:76905730-76906044	HepG2	liver:	n/a	chr16:76905880-76905891
46	CEBPB	chr16:76825079-76825413	HepG2	liver:	n/a	chr16:76825240-76825251
47	CEBPB	chr16:77004639-77004999	HepG2	liver:	n/a	n/a
48	CEBPB	chr16:76946642-76947268	A549	lung:	n/a	chr16:76946917-76946930 chr16:76946917-76946930 chr16:76946918-76946929
49	CEBPB	chr16:76905764-76905938	IMR90	lung:	n/a	chr16:76905880-76905891
50	CEBPB	chr16:76814500-76814768	MCF-7	breast:	n/a	n/a

No data

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:76817240..76820216-chr16:76820936..76823507,2	K562	blood:
2	chr16:76773881..76775450-chr16:76881262..76882791,2	MCF-7	breast:
3	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
4	chr16:76844876..76847420-chr19:45599129..45600971,2	MCF-7	breast:
5	chr16:76972133..76974493-chr16:76974679..76976840,2	MCF-7	breast:
6	chr16:76856883..76857419-chr16:77076804..77077643,2	MCF-7	breast:
7	chr16:76878928..76880909-chr16:76882753..76884640,2	K562	blood:
8	chr16:77059610..77062396-chr16:77260233..77262257,2	K562	blood:
9	chr16:76817240..76820216-chr16:76820936..76823507,2	K562	blood:
10	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
11	chr16:76886880..76887748-chr16:77077328..77078325,2	MCF-7	breast:
12	chr16:76846196..76848121-chr16:76848521..76851117,2	MCF-7	breast:
13	chr16:76887878..76888800-chr16:77205307..77205910,4	MCF-7	breast:
14	chr16:76846196..76848121-chr16:76848521..76851117,2	MCF-7	breast:
15	chr16:76881611..76883954-chr16:76887729..76889678,2	MCF-7	breast:
16	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
17	chr16:76881611..76883954-chr16:76887729..76889678,2	MCF-7	breast:
18	chr16:76887924..76888465-chr16:77203271..77204023,2	MCF-7	breast:
19	chr16:76972133..76974493-chr16:76974679..76976840,2	MCF-7	breast:
20	chr16:76887896..76888842-chr16:77076469..77077719,11	MCF-7	breast:
21	chr16:76856883..76857419-chr16:77076804..77077643,2	MCF-7	breast:
22	chr16:77044641..77046687-chr16:77049304..77051697,2	K562	blood:
23	chr16:76887394..76888672-chr16:77203188..77204165,5	MCF-7	breast:
24	chr16:77044641..77046687-chr16:77049304..77051697,2	K562	blood:
25	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
26	chr16:76878928..76880909-chr16:76882753..76884640,2	K562	blood:
27	chr16:76887896..76888842-chr16:77076469..77077719,11	MCF-7	breast:
28	chr16:77078662..77079429-chr16:77203303..77204211,3	MCF-7	breast:
29	chr16:77076688..77077729-chr16:77203577..77204202,3	MCF-7	breast:
30	chr16:76886880..76887748-chr16:77077328..77078325,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAMTS18-8	chr16:76912171-76912833	NONHSAT143788
2	lnc-RP11-58C22.1.1-3	chr16:76806570-76806959	XLOC_011793
3	lnc-RP11-58C22.1.1-4	chr16:76961793-76962066	ENSG00000259995.1
4	lnc-ADAMTS18-2	chr16:77042061-77042204	XLOC_012014
5	lnc-ADAMTS18-2	chr16:77028205-77028433	XLOC_012014
6	lnc-RP11-58C22.1.1-3	chr16:76803213-76803278	XLOC_011793
7	lnc-RP11-58C22.1.1-4	chr16:76946252-76946305	ENSG00000259995.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4719	chr16:76902885-76902906	MIMAT0019832

No data

Variant related genes	Relation type
ENSG00000260797	TF binding region
MIR4719	TF binding region
PYGO2	miRNA target sites
QARS	miRNA target sites

Extended variants
information (count: 8330 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:8330 , 50 per page) page: 1 2 3 4 5 6 7 ... 167

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs68127547	chr16:76781201-76781202	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35092808	chr16:76781237-76781238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs193075674	chr16:76781254-76781255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79658890	chr16:76781262-76781263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554258189	chr16:76781280-76781281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185661869	chr16:76781338-76781339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187782688	chr16:76781341-76781342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563000017	chr16:76781356-76781357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377749445	chr16:76781376-76781377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532022597	chr16:76781427-76781428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35944588	chr16:76781450-76781451	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs375703990	chr16:76781533-76781534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556210355	chr16:76781542-76781543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561646786	chr16:76781573-76781574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368198512	chr16:76781613-76781614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548978500	chr16:76781616-76781617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114070076	chr16:76781637-76781638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138177032	chr16:76781643-76781644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527878236	chr16:76781645-76781646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74876924	chr16:76781663-76781664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546303971	chr16:76781687-76781688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547479709	chr16:76781706-76781707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570548016	chr16:76781720-76781721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191489697	chr16:76781724-76781725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183607738	chr16:76781730-76781731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573830191	chr16:76781734-76781735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115052295	chr16:76781750-76781751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149510815	chr16:76781826-76781827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542241116	chr16:76781836-76781837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200435927	chr16:76781878-76781879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143995510	chr16:76781881-76781882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568081739	chr16:76781900-76781901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148661622	chr16:76781922-76781923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78326200	chr16:76781936-76781937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112882693	chr16:76781965-76781966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188271115	chr16:76781994-76781995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577280510	chr16:76781996-76781997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546021363	chr16:76782039-76782040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556715313	chr16:76782051-76782052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542956492	chr16:76782081-76782082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542526246	chr16:76782128-76782129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562382048	chr16:76782145-76782146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527250051	chr16:76782163-76782164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs117034552	chr16:76782223-76782224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs60056123	chr16:76782268-76782269	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs550661174	chr16:76782283-76782284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374985646	chr16:76782308-76782309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563982860	chr16:76782314-76782315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533035195	chr16:76782321-76782322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs61217580	chr16:76782360-76782361	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

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
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Lung cancer	24585490	CNVD
Neuroblastoma	18923524	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20581869	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76781200-76781600	Enhancers	Brain Germinal Matrix	brain
2	chr16:76781200-76784800	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr16:76781600-76782800	Weak transcription	Brain Germinal Matrix	brain
4	chr16:76782200-76785400	Enhancers	Fetal Lung	lung
5	chr16:76782600-76783800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr16:76782800-76784000	Enhancers	Brain Germinal Matrix	brain
7	chr16:76783000-76783200	Enhancers	Gastric	stomach
8	chr16:76783800-76784200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr16:76784000-76786400	Weak transcription	Brain Germinal Matrix	brain
10	chr16:76784200-76784600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr16:76784400-76784600	Enhancers	Fetal Brain Male	brain
12	chr16:76784600-76785600	Weak transcription	Fetal Brain Male	brain
13	chr16:76784800-76785200	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr16:76785200-76785800	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr16:76785600-76787400	Enhancers	Fetal Brain Male	brain
16	chr16:76786400-76787000	Enhancers	Brain Germinal Matrix	brain
17	chr16:76788200-76789000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr16:76797200-76797600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr16:76802400-76802800	Enhancers	Colon Smooth Muscle	Colon
20	chr16:76802800-76803200	Enhancers	Stomach Smooth Muscle	stomach
21	chr16:76803600-76803800	Enhancers	Fetal Brain Male	brain
22	chr16:76803800-76804400	Weak transcription	Fetal Brain Male	brain
23	chr16:76804400-76807000	Enhancers	Fetal Brain Male	brain
24	chr16:76805000-76805600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr16:76805000-76806000	Enhancers	Fetal Brain Female	brain
26	chr16:76805200-76805600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr16:76808800-76812200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr16:76811600-76812000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr16:76811600-76812400	Enhancers	Brain Germinal Matrix	brain
30	chr16:76811800-76812600	Enhancers	HMEC	breast
31	chr16:76812000-76812400	Enhancers	Fetal Brain Female	brain
32	chr16:76812000-76813000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr16:76812200-76812600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr16:76812600-76813800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr16:76812600-76818000	Weak transcription	HMEC	breast
36	chr16:76813000-76818800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr16:76813200-76813400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr16:76813400-76816800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr16:76813800-76814400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr16:76814400-76815000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr16:76815000-76815200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr16:76815200-76817600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr16:76816800-76818600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr16:76817600-76818200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr16:76818000-76819000	Enhancers	HMEC	breast
46	chr16:76818200-76824000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr16:76819000-76821000	Weak transcription	HMEC	breast
48	chr16:76821000-76821400	Enhancers	HMEC	breast
49	chr16:76824000-76824200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr16:76824200-76838800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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