Variant report

Variant	esv3430225
Chromosome Location	chr16:71633500-71661205
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:812)
CpG islands
(count:732)
Chromatin interactive
region (count:37)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:812 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:71642132-71642725	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:71634694-71634912	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:71644905-71645340	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:71657501-71657779	HepG2	liver:	n/a	n/a
5	ATF2	chr16:71642058-71642791	GM12878	blood:	n/a	n/a
6	ATF2	chr16:71641887-71642800	GM12878	blood:	n/a	n/a
7	ATF3	chr16:71659855-71660233	HepG2	liver:	n/a	chr16:71660046-71660055 chr16:71660041-71660050 chr16:71660124-71660132
8	BATF	chr16:71642193-71642801	GM12878	blood:	n/a	chr16:71642358-71642368
9	BATF	chr16:71641662-71642761	GM12878	blood:	n/a	chr16:71642358-71642368
10	BCL11A	chr16:71642216-71642692	GM12878	blood:	n/a	chr16:71642357-71642366 chr16:71642377-71642386
11	BCL11A	chr16:71641659-71642790	GM12878	blood:	n/a	chr16:71642357-71642366 chr16:71642377-71642386
12	BCL3	chr16:71642147-71642729	GM12878	blood:	n/a	chr16:71642357-71642366 chr16:71642377-71642386
13	BCLAF1	chr16:71642147-71642714	GM12878	blood:	n/a	chr16:71642357-71642366 chr16:71642377-71642386
14	BCLAF1	chr16:71642238-71642804	GM12878	blood:	n/a	chr16:71642357-71642366 chr16:71642377-71642386
15	BHLHE40	chr16:71641692-71642735	GM12878	blood:	n/a	n/a
16	BHLHE40	chr16:71644964-71645268	K562	blood:	n/a	n/a
17	BRCA1	chr16:71644983-71645175	HepG2	liver:	n/a	n/a
18	BRCA1	chr16:71645032-71645044	GM12878	blood:	n/a	n/a
19	CEBPB	chr16:71642223-71642618	GM12878	blood:	n/a	n/a
20	CEBPB	chr16:71641963-71642825	GM12878	blood:	n/a	n/a
21	CEBPB	chr16:71644867-71645001	K562	blood:	n/a	n/a
22	CEBPB	chr16:71641420-71641644	HepG2	liver:	n/a	chr16:71641517-71641528
23	CEBPB	chr16:71644471-71644632	HepG2	liver:	n/a	n/a
24	CEBPB	chr16:71633581-71633600	K562	blood:	n/a	n/a
25	CEBPB	chr16:71644519-71644575	K562	blood:	n/a	n/a
26	CEBPB	chr16:71644463-71644579	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr16:71634597-71634944	HepG2	liver:	n/a	chr16:71634752-71634763
28	CEBPB	chr16:71633516-71633709	A549	lung:	n/a	chr16:71633551-71633562
29	CEBPB	chr16:71641465-71641567	A549	lung:	n/a	chr16:71641517-71641528
30	CEBPB	chr16:71634691-71634784	HepG2	liver:	n/a	chr16:71634752-71634763
31	CEBPB	chr16:71633476-71633714	HepG2	liver:	n/a	chr16:71633551-71633562
32	CHD1	chr16:71642097-71642668	GM12878	blood:	n/a	n/a
33	CHD1	chr16:71660207-71660850	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr16:71644851-71645250	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr16:71644930-71645255	HepG2	liver:	n/a	n/a
36	CHD2	chr16:71644874-71645251	GM12878	blood:	n/a	n/a
37	CHD2	chr16:71644920-71645221	K562	blood:	n/a	n/a
38	CHD2	chr16:71642197-71642656	GM12878	blood:	n/a	n/a
39	CHD2	chr16:71659838-71660253	H1-hESC	embryonic stem cell:	n/a	chr16:71660044-71660054
40	CREB1	chr16:71644958-71645316	A549	lung:	n/a	n/a
41	CREB1	chr16:71641976-71642820	GM12878	blood:	n/a	n/a
42	CTCF	chr16:71659920-71660070	HepG2	liver:	n/a	chr16:71659979-71659992
43	CTCF	chr16:71645060-71645210	HBMEC	blood vessel:	n/a	chr16:71645089-71645107 chr16:71645095-71645104 chr16:71645113-71645126 chr16:71645091-71645104 chr16:71645084-71645105
44	CTCF	chr16:71645040-71645190	HEK293	kidney:	n/a	chr16:71645089-71645107 chr16:71645095-71645104 chr16:71645113-71645126 chr16:71645091-71645104 chr16:71645084-71645105
45	CTCF	chr16:71644832-71645355	A549	lung:	n/a	chr16:71645089-71645107 chr16:71645095-71645104 chr16:71645113-71645126 chr16:71645091-71645104 chr16:71645084-71645105
46	CTCF	chr16:71645040-71645190	RPTEC	kidney:	n/a	chr16:71645089-71645107 chr16:71645095-71645104 chr16:71645113-71645126 chr16:71645091-71645104 chr16:71645084-71645105
47	CTCF	chr16:71644950-71645233	MCF-7	breast:	n/a	chr16:71645089-71645107 chr16:71645095-71645104 chr16:71645113-71645126 chr16:71645091-71645104 chr16:71645084-71645105
48	CTCF	chr16:71645040-71645190	GM12873	blood:	n/a	chr16:71645089-71645107 chr16:71645095-71645104 chr16:71645113-71645126 chr16:71645091-71645104 chr16:71645084-71645105
49	CTCF	chr16:71645543-71645636	MCF-7	breast:	n/a	n/a
50	CTCF	chr16:71641680-71641830	GM12875	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:71660103-71660153	AoSMC	blood vessel:	n/a
2	chr16:71660055-71660105	PANC-1	pancreas:	n/a
3	chr16:71660022-71660072	HMEC	breast:	n/a
4	chr16:71660049-71660099	HRE	kidney:	n/a
5	chr16:71659830-71659880	HepG2	liver:	n/a
6	chr16:71660463-71660513	HCT-116	colon:	n/a
7	chr16:71660049-71660099	AG09309	skin:	n/a
8	chr16:71659830-71659880	BE2_C	brain:	n/a
9	chr16:71660103-71660153	NT2-D1	testis:	n/a
10	chr16:71660044-71660094	H1-hESC	embryonic stem cell:	embryo
11	chr16:71660734-71660784	GM19239	blood:	n/a
12	chr16:71659830-71659880	NB4	blood:	n/a
13	chr16:71660103-71660153	GM19239	blood:	n/a
14	chr16:71657362-71657412	NHDF-neo	bronchial:	n/a
15	chr16:71658155-71658205	HIPEpiC	eye:	n/a
16	chr16:71657362-71657412	AG04449	skin:	fetal
17	chr16:71660022-71660072	Hepatocyte	liver:	n/a
18	chr16:71660463-71660513	A549	lung:	n/a
19	chr16:71660908-71660958	RPTEC	kidney:	n/a
20	chr16:71660055-71660105	HRCEpiC	kidney:	n/a
21	chr16:71660044-71660094	HRE	kidney:	n/a
22	chr16:71660734-71660784	PrEC	prostate:	n/a
23	chr16:71660049-71660099	Jurkat	blood:	n/a
24	chr16:71660113-71660163	SK-N-SH	brain:	n/a
25	chr16:71660103-71660153	GM12878	blood:	n/a
26	chr16:71660463-71660513	GM06990	blood:	n/a
27	chr16:71660113-71660163	BE2_C	brain:	n/a
28	chr16:71660908-71660958	NHBE	bronchial:	n/a
29	chr16:71660049-71660099	K562	blood:	n/a
30	chr16:71660044-71660094	CMK	blood:	n/a
31	chr16:71660044-71660094	HCM	heart:	n/a
32	chr16:71660463-71660513	HAEpiC	amniotic membrane:	n/a
33	chr16:71660463-71660513	AG04450	lung:	fetal
34	chr16:71660734-71660784	HEEpiC	esophagus:	n/a
35	chr16:71658155-71658205	LNCaP	prostate:	n/a
36	chr16:71660049-71660099	HPAEpiC	pulmonary alveolar:	n/a
37	chr16:71660113-71660163	GM12891	blood:	n/a
38	chr16:71660908-71660958	GM06990	blood:	n/a
39	chr16:71660113-71660163	PANC-1	pancreas:	n/a
40	chr16:71660055-71660105	NHDF-neo	bronchial:	n/a
41	chr16:71660049-71660099	H1-hESC	embryonic stem cell:	embryo
42	chr16:71660734-71660784	AG04450	lung:	fetal
43	chr16:71660044-71660094	BJ	skin:	n/a
44	chr16:71657362-71657412	GM12878	blood:	n/a
45	chr16:71660055-71660105	HL-60	blood:	n/a
46	chr16:71660734-71660784	AG10803	skin:	n/a
47	chr16:71660908-71660958	HRCEpiC	kidney:	n/a
48	chr16:71660022-71660072	AG09319	gingival:	n/a
49	chr16:71660463-71660513	MCF-7	breast:	n/a
50	chr16:71660022-71660072	SKMC	muscle:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:71649063..71651732-chr16:71653397..71655968,3	MCF-7	breast:
2	chr16:71536485..71537281-chr16:71644648..71645398,2	MCF-7	breast:
3	chr16:71598139..71600865-chr16:71657563..71661455,3	MCF-7	breast:
4	chr16:71533780..71534445-chr16:71644552..71645471,2	MCF-7	breast:
5	chr10:75757141..75757912-chr16:71659926..71660540,2	HCT-116	colon:
6	chr16:71598501..71600044-chr16:71644493..71645682,11	MCF-7	breast:
7	chr16:71652939..71655689-chr16:71657502..71661086,3	K562	blood:
8	chr16:71598932..71599494-chr16:71644689..71645368,2	K562	blood:
9	chr16:71634121..71636611-chr16:71640952..71642935,2	MCF-7	breast:
10	chr16:71598437..71599429-chr16:71641387..71642200,2	MCF-7	breast:
11	chr16:71634121..71636611-chr16:71640952..71642935,2	MCF-7	breast:
12	chr16:71639360..71642316-chr16:71645937..71648287,2	K562	blood:
13	chr16:71659983..71661516-chr16:71697596..71700523,2	MCF-7	breast:
14	chr16:71586592..71587218-chr16:71644906..71645667,2	MCF-7	breast:
15	chr16:71597182..71598726-chr16:71654559..71657394,2	MCF-7	breast:
16	chr16:71446366..71447179-chr16:71644599..71645567,3	K562	blood:
17	chr16:71649063..71651732-chr16:71653397..71655968,3	MCF-7	breast:
18	chr16:71598966..71599999-chr16:71641229..71642599,6	MCF-7	breast:
19	chr16:71639360..71642316-chr16:71645937..71648287,2	K562	blood:
20	chr16:71567921..71569617-chr16:71645011..71646646,2	MCF-7	breast:
21	chr16:71644641..71645674-chr16:71679043..71680015,5	MCF-7	breast:
22	chr16:71659512..71660044-chr16:71679141..71679971,2	MCF-7	breast:
23	chr16:71645072..71647361-chr16:71660009..71661728,2	MCF-7	breast:
24	chr16:71598829..71599535-chr16:71644892..71645491,2	MCF-7	breast:
25	chr16:71660779..71663588-chr16:71917487..71919954,2	MCF-7	breast:
26	chr16:71597451..71600395-chr16:71660172..71663639,3	MCF-7	breast:
27	chr16:71598913..71599557-chr16:71641715..71642369,2	MCF-7	breast:
28	chr16:71658952..71666464-chr16:71755738..71760832,8	MCF-7	breast:
29	chr16:71645006..71646699-chr16:71648502..71650487,2	MCF-7	breast:
30	chr16:71647960..71650454-chr16:71756899..71758673,2	MCF-7	breast:
31	chr16:71596573..71599590-chr16:71642907..71646466,3	MCF-7	breast:
32	chr16:71540507..71541058-chr16:71644975..71645549,2	K562	blood:
33	chr16:71515385..71518984-chr16:71658944..71661712,3	MCF-7	breast:
34	chr16:71644466..71645406-chr16:71995435..71996080,2	K562	blood:
35	chr16:71645006..71646699-chr16:71648502..71650487,2	MCF-7	breast:
36	chr16:71446668..71447388-chr16:71644674..71645331,3	MCF-7	breast:
37	chr16:71576269..71576821-chr16:71644589..71645172,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHLPP2-1	chr16:71660501-71660719	ENSG00000260593.1
2	lnc-PHLPP2-1	chr16:71657611-71657856	ENSG00000260593.1

No data

Variant related genes	Relation type
MARVELD3	TF binding region
ENSG00000260593	TF binding region
MARVELD3	CpG island
ENSG00000260593	CpG island
ENSG00000252339	chromatin interactions
ENSG00000140832	chromatin interactions
ENSG00000260886	chromatin interactions
ENSG00000261513	chromatin interactions
ENSG00000035403	chromatin interactions
ENSG00000260593	chromatin interactions
ENSG00000199301	chromatin interactions
ENSG00000157429	chromatin interactions
ENSG00000182149	chromatin interactions
ENSG00000040199	chromatin interactions
ENSG00000102984	chromatin interactions

Extended variants
information (count: 1054 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1054 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561185139	chr16:71633512-71633513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573148787	chr16:71633538-71633539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150659166	chr16:71633583-71633584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559661553	chr16:71633584-71633585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs8044269	chr16:71633605-71633606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs17282500	chr16:71633653-71633654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs531730368	chr16:71633661-71633662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563572517	chr16:71633678-71633679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547350101	chr16:71633765-71633766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531023093	chr16:71633794-71633795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549136431	chr16:71633796-71633797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529578275	chr16:71633810-71633811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567621380	chr16:71633824-71633825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184913256	chr16:71633855-71633856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190205825	chr16:71633862-71633863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9940142	chr16:71633873-71633874	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs376508118	chr16:71633904-71633905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550346830	chr16:71633961-71633962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538384329	chr16:71633967-71633968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557004253	chr16:71633973-71633974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529533254	chr16:71633978-71633979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549411143	chr16:71633985-71633986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575377805	chr16:71633986-71633987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182435840	chr16:71634020-71634021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554760123	chr16:71634110-71634111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569259006	chr16:71634128-71634129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540514484	chr16:71634129-71634130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs8045236	chr16:71634168-71634169	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs577952598	chr16:71634223-71634224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545037899	chr16:71634256-71634257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186603234	chr16:71634268-71634269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530865593	chr16:71634279-71634280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200413048	chr16:71634296-71634297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549174989	chr16:71634363-71634364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561137041	chr16:71634373-71634374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190331104	chr16:71634414-71634415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557862526	chr16:71634423-71634424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117991390	chr16:71634433-71634434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371751227	chr16:71634464-71634465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145605728	chr16:71634498-71634499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532150717	chr16:71634525-71634526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550568364	chr16:71634543-71634544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4788547	chr16:71634544-71634545	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs181200385	chr16:71634562-71634563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554847900	chr16:71634596-71634597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4788814	chr16:71634604-71634605	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs533875264	chr16:71634606-71634607	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185609613	chr16:71634679-71634680	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35313639	chr16:71634708-71634709	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148911751	chr16:71634777-71634778	Flanking Active TSS Enhancers Weak transcription	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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	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 myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Neuroblastoma	18923524	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:465 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71630400-71634400	Weak transcription	Liver	Liver
2	chr16:71632600-71634800	Weak transcription	A549	lung
3	chr16:71633400-71634400	Weak transcription	HepG2	liver
4	chr16:71634400-71634600	Enhancers	Liver	Liver
5	chr16:71634400-71634600	Enhancers	HepG2	liver
6	chr16:71634600-71634800	Flanking Active TSS	Liver	Liver
7	chr16:71634600-71634800	Enhancers	Brain Substantia Nigra	brain
8	chr16:71634600-71635200	Enhancers	Brain Hippocampus Middle	brain
9	chr16:71634600-71635200	Flanking Active TSS	HepG2	liver
10	chr16:71634800-71635000	Enhancers	Liver	Liver
11	chr16:71634800-71635000	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr16:71634800-71635200	Enhancers	Brain Cingulate Gyrus	brain
13	chr16:71634800-71635200	Enhancers	A549	lung
14	chr16:71635000-71635200	Flanking Active TSS	Liver	Liver
15	chr16:71635200-71635400	Enhancers	Liver	Liver
16	chr16:71635200-71640600	Weak transcription	HepG2	liver
17	chr16:71640600-71642000	Enhancers	HepG2	liver
18	chr16:71641000-71641200	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr16:71641000-71641600	Enhancers	GM12878-XiMat	blood
20	chr16:71641000-71642200	Weak transcription	A549	lung
21	chr16:71641200-71641400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr16:71641200-71644800	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr16:71641400-71642400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr16:71641600-71641800	Enhancers	Placenta	Placenta
25	chr16:71641600-71642000	Enhancers	Lung	lung
26	chr16:71641600-71642000	Weak transcription	GM12878-XiMat	blood
27	chr16:71641800-71644800	Weak transcription	Placenta	Placenta
28	chr16:71642000-71642200	Flanking Active TSS	HepG2	liver
29	chr16:71642000-71642800	Enhancers	NH-A	brain
30	chr16:71642000-71645400	Enhancers	GM12878-XiMat	blood
31	chr16:71642200-71642600	Enhancers	A549	lung
32	chr16:71642200-71642800	Enhancers	HepG2	liver
33	chr16:71642200-71643600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr16:71642400-71642600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr16:71642400-71642600	Enhancers	H9 Cell Line	embryonic stem cell
36	chr16:71642400-71642600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr16:71642400-71642600	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr16:71642600-71642800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr16:71642600-71643000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr16:71642600-71644800	Weak transcription	A549	lung
41	chr16:71642800-71644800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr16:71642800-71644800	Weak transcription	HepG2	liver
43	chr16:71642800-71645200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr16:71643000-71644800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr16:71643000-71644800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr16:71643200-71643800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr16:71643600-71644800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr16:71643800-71644800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr16:71644200-71644800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr16:71644200-71647600	Weak transcription	Right Atrium	heart

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