Variant report

Variant	nsv1017498
Chromosome Location	chr7:16262300-16313476
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:517)
CpG islands
(count:0)
Chromatin interactive
region (count:39)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:517 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:16299083-16299409	K562	blood:	n/a	n/a
2	ARID3A	chr7:16302411-16302607	K562	blood:	n/a	n/a
3	ARID3A	chr7:16299684-16300431	K562	blood:	n/a	n/a
4	ARID3A	chr7:16300636-16301991	K562	blood:	n/a	n/a
5	ARID3A	chr7:16304739-16305925	K562	blood:	n/a	n/a
6	ARID3A	chr7:16307063-16308041	K562	blood:	n/a	n/a
7	ARID3A	chr7:16308350-16309290	K562	blood:	n/a	n/a
8	ATF1	chr7:16301437-16301703	K562	blood:	n/a	n/a
9	ATF1	chr7:16300049-16300351	K562	blood:	n/a	n/a
10	ATF1	chr7:16266719-16266733	K562	blood:	n/a	n/a
11	ATF1	chr7:16304760-16305221	K562	blood:	n/a	n/a
12	ATF1	chr7:16308377-16309311	K562	blood:	n/a	n/a
13	ATF3	chr7:16308269-16309108	K562	blood:	n/a	n/a
14	BCL3	chr7:16308310-16309048	K562	blood:	n/a	n/a
15	BCLAF1	chr7:16308322-16309035	K562	blood:	n/a	n/a
16	BCLAF1	chr7:16305341-16306186	K562	blood:	n/a	n/a
17	BCLAF1	chr7:16301267-16301844	K562	blood:	n/a	n/a
18	BCLAF1	chr7:16308244-16309056	K562	blood:	n/a	n/a
19	BHLHE40	chr7:16297424-16297442	K562	blood:	n/a	n/a
20	BHLHE40	chr7:16306312-16306532	K562	blood:	n/a	n/a
21	BHLHE40	chr7:16304830-16305615	K562	blood:	n/a	n/a
22	BHLHE40	chr7:16303074-16303109	K562	blood:	n/a	n/a
23	BHLHE40	chr7:16308296-16309332	K562	blood:	n/a	n/a
24	CBX3	chr7:16271850-16272277	K562	blood:	n/a	n/a
25	CBX3	chr7:16269828-16270194	K562	blood:	n/a	n/a
26	CBX3	chr7:16308343-16309472	K562	blood:	n/a	n/a
27	CBX3	chr7:16295561-16295958	K562	blood:	n/a	n/a
28	CBX3	chr7:16269898-16270150	K562	blood:	n/a	n/a
29	CBX3	chr7:16312862-16313345	K562	blood:	n/a	n/a
30	CBX3	chr7:16308325-16309283	K562	blood:	n/a	n/a
31	CCNT2	chr7:16308074-16309185	K562	blood:	n/a	n/a
32	CCNT2	chr7:16304676-16305206	K562	blood:	n/a	n/a
33	CCNT2	chr7:16310417-16310723	K562	blood:	n/a	n/a
34	CCNT2	chr7:16301397-16301732	K562	blood:	n/a	n/a
35	CCNT2	chr7:16299875-16300334	K562	blood:	n/a	n/a
36	CEBPB	chr7:16274104-16274388	K562	blood:	n/a	n/a
37	CEBPB	chr7:16304474-16304690	K562	blood:	n/a	n/a
38	CEBPB	chr7:16308357-16309029	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:16304794-16305678	K562	blood:	n/a	n/a
40	CEBPB	chr7:16304910-16305502	K562	blood:	n/a	n/a
41	CEBPB	chr7:16299062-16299191	K562	blood:	n/a	n/a
42	CEBPB	chr7:16299779-16300445	K562	blood:	n/a	n/a
43	CEBPB	chr7:16308212-16309353	K562	blood:	n/a	n/a
44	CEBPB	chr7:16305889-16305921	K562	blood:	n/a	n/a
45	CEBPB	chr7:16308306-16309211	K562	blood:	n/a	n/a
46	CEBPB	chr7:16279656-16279856	HepG2	liver:	n/a	chr7:16279790-16279801
47	CEBPB	chr7:16308351-16308943	K562	blood:	n/a	n/a
48	CEBPB	chr7:16285457-16285721	HepG2	liver:	n/a	chr7:16285552-16285563
49	CEBPB	chr7:16301287-16301995	K562	blood:	n/a	n/a
50	CEBPD	chr7:16308218-16309234	K562	blood:	n/a	n/a

No data

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:16304631..16307990-chr7:16437547..16440554,3	K562	blood:
2	chr7:16304973..16307091-chr7:16435445..16437043,2	K562	blood:
3	chr7:16272248..16275452-chr7:16305157..16308165,4	K562	blood:
4	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
5	chr7:16307737..16311020-chr7:16684818..16687152,3	K562	blood:
6	chr7:16301403..16303759-chr7:16503630..16506930,3	K562	blood:
7	chr7:12753228..12755385-chr7:16301600..16303385,2	K562	blood:
8	chr7:16271837..16274588-chr7:16275186..16279473,3	K562	blood:
9	chr7:16272248..16274869-chr7:16305157..16307096,2	K562	blood:
10	chr7:16263097..16266771-chr7:16270720..16274586,3	K562	blood:
11	chr7:16303209..16307181-chr7:16682528..16687363,4	K562	blood:
12	chr7:16272248..16275452-chr7:16305157..16308165,4	K562	blood:
13	chr7:16301478..16303849-chr7:16518183..16519712,2	K562	blood:
14	chr7:16285409..16288180-chr7:16295653..16298089,2	K562	blood:
15	chr7:16221967..16224628-chr7:16306153..16308389,2	K562	blood:
16	chr7:16302978..16309646-chr7:16456908..16462647,13	K562	blood:
17	chr7:16277063..16278861-chr7:16280781..16282424,2	K562	blood:
18	chr7:16297813..16300771-chr7:16597599..16599779,2	K562	blood:
19	chr7:16277063..16278675-chr7:16280781..16282945,2	K562	blood:
20	chr7:16300347..16301994-chr7:16462021..16464400,2	K562	blood:
21	chr7:16271772..16276074-chr7:16279630..16282231,4	K562	blood:
22	chr7:16307891..16309646-chr7:16460887..16462647,2	K562	blood:
23	chr7:16285409..16288180-chr7:16295653..16298089,2	K562	blood:
24	chr7:16271772..16276074-chr7:16279630..16282231,4	K562	blood:
25	chr7:16302428..16304569-chr7:16686662..16689057,2	K562	blood:
26	chr7:16277063..16278675-chr7:16280781..16282945,2	K562	blood:
27	chr7:16277063..16278861-chr7:16280781..16282424,2	K562	blood:
28	chr7:16274806..16276431-chr7:16298235..16300903,2	K562	blood:
29	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
30	chr7:16165242..16168046-chr7:16300329..16302056,2	K562	blood:
31	chr7:16307417..16309237-chr7:16685352..16687215,2	K562	blood:
32	chr7:16302626..16306339-chr7:16456665..16460333,5	K562	blood:
33	chr7:16272248..16274869-chr7:16305157..16307096,2	K562	blood:
34	chr7:16263097..16266771-chr7:16270720..16274586,3	K562	blood:
35	chr7:16275733..16277560-chr7:16684679..16686192,2	K562	blood:
36	chr7:16271837..16274588-chr7:16275186..16279473,3	K562	blood:
37	chr7:16274806..16276431-chr7:16298235..16300903,2	K562	blood:
38	chr7:16301506..16303412-chr7:20253971..20256529,2	K562	blood:
39	chr7:16309917..16312167-chr7:16461370..16463570,2	K562	blood:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119294
2	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119293
3	lnc-AC006035.2-1	chr7:16301524-16301721	NONHSAT119293
4	lnc-AC006035.2-1	chr7:16272377-16272461	ucscGeneNc_uc003stf_2
5	lnc-AC006035.2-1	chr7:16305852-16305936	ENSG00000229688
6	lnc-AC006035.2-1	chr7:16288360-16288362	NONHSAT119294
7	lnc-AC006035.2-1	chr7:16275527-16275604	ENSG00000229688
8	lnc-AC006035.2-1	chr7:16308482-16310229	ENSG00000229688
9	lnc-AC006035.2-1	chr7:16268049-16268246	ucscGeneNc_uc003stf_2
10	lnc-AC006035.2-1	chr7:16276934-16277038	NONHSAT119293
11	lnc-AC006035.2-1	chr7:16275527-16275604	NONHSAT119295
12	lnc-AC006035.2-1	chr7:16276934-16277038	NONHSAT119294
13	lnc-AC006035.2-1	chr7:16276934-16276977	ENSG00000229688
14	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119295
15	lnc-AC006035.2-1	chr7:16287510-16287714	ENSG00000229688.3
16	lnc-AC006035.2-1	chr7:16301524-16301721	ENSG00000229688
17	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119292
18	lnc-AC006035.2-1	chr7:16308482-16309502	NONHSAT119295
19	lnc-AC006035.2-1	chr7:16276934-16277031	ENSG00000229688.3
20	lnc-AC006035.2-1	chr7:16276934-16277038	ENSG00000229688
21	lnc-AC006035.2-1	chr7:16301527-16301721	NONHSAT119294
22	lnc-AC006035.2-1	chr7:16276934-16277035	NONHSAT119295
23	lnc-AC006035.2-1	chr7:16276934-16276977	NONHSAT119292
24	lnc-AC006035.2-1	chr7:16275007-16276752	ucscGeneNc_uc003stf_2
25	lnc-AC006035.2-1	chr7:16308874-16309215	ENSG00000241044
26	lnc-AC006035.2-1	chr7:16305852-16305936	ENSG00000229688
27	lnc-AC006035.2-1	chr7:16308482-16308872	ENSG00000229688
28	lnc-AC006035.2-1	chr7:16308482-16310229	NONHSAT119293
29	lnc-AC006035.2-1	chr7:16276934-16277035	ENSG00000229688.3
30	lnc-AC006035.2-1	chr7:16275527-16275604	NONHSAT119292
31	lnc-AC006035.2-1	chr7:16308482-16310229	NONHSAT119294
32	lnc-AC006035.2-1	chr7:16310142-16310229	ENSG00000241044
33	lnc-AC006035.2-1	chr7:16308482-16309502	NONHSAT119296
34	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119296
35	lnc-AC006035.2-1	chr7:16310630-16310643	NONHSAT119294
36	lnc-AC006035.2-1	chr7:16308482-16310229	NONHSAT119292

No data

Variant related genes	Relation type
ISPD-AS1	TF binding region
ENSG00000214960	chromatin interactions
ENSG00000136261	chromatin interactions
ENSG00000171243	chromatin interactions
ENSG00000106524	chromatin interactions
DIS3L	miRNA target sites
RSRC2	miRNA target sites
SEC63	miRNA target sites
LMLN	miRNA target sites
GLTP	miRNA target sites
TTC8	miRNA target sites
CDKN1B	miRNA target sites
HAS3	miRNA target sites

Extended variants
information (count: 2136 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2136 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188256082	chr7:16262309-16262310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370971618	chr7:16262360-16262361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12216621	chr7:16262371-16262372	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs191003108	chr7:16262410-16262411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574829570	chr7:16262419-16262420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183312046	chr7:16262428-16262429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568908644	chr7:16262432-16262433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187266455	chr7:16262501-16262502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114793728	chr7:16262522-16262523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572881229	chr7:16262524-16262525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534050933	chr7:16262601-16262602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs118020202	chr7:16262605-16262606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138936916	chr7:16262640-16262641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544101645	chr7:16262652-16262653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562995450	chr7:16262659-16262660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143450414	chr7:16262669-16262670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545491609	chr7:16262680-16262681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555148694	chr7:16262737-16262738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544643909	chr7:16262738-16262739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145791996	chr7:16262767-16262768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138621516	chr7:16262816-16262817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192197190	chr7:16262824-16262825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142757062	chr7:16262827-16262828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531932889	chr7:16262837-16262838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540505402	chr7:16262841-16262842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74901096	chr7:16262857-16262858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34772536	chr7:16262910-16262911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571821940	chr7:16263065-16263066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539116903	chr7:16263102-16263103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551520310	chr7:16263141-16263142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs57179130	chr7:16263161-16263162	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs533803839	chr7:16263203-16263204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555677454	chr7:16263206-16263207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77029597	chr7:16263225-16263226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4721481	chr7:16263268-16263269	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs538033950	chr7:16263291-16263292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111839579	chr7:16263321-16263322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77652916	chr7:16263327-16263328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184610598	chr7:16263365-16263366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576496526	chr7:16263374-16263375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545137564	chr7:16263396-16263397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560247667	chr7:16263434-16263435	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572087901	chr7:16263452-16263453	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34194782	chr7:16263505-16263506	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs398111101	chr7:16263514-16263515	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79161846	chr7:16263528-16263529	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187884155	chr7:16263531-16263532	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531871435	chr7:16263594-16263595	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531826459	chr7:16263606-16263607	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113934026	chr7:16263615-16263616	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	19805367	CNVD
Autism	20808228	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16250200-16275800	Weak transcription	Pancreas	Pancrea
2	chr7:16262600-16263000	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr7:16262600-16263400	Enhancers	Primary T cells from cord blood	blood
4	chr7:16262600-16263400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr7:16262600-16263800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr7:16262600-16264200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr7:16262600-16264400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr7:16262600-16264800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr7:16263000-16263400	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr7:16263000-16264200	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr7:16263200-16264200	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr7:16263200-16264200	Enhancers	Dnd41	blood
13	chr7:16263400-16263800	Active TSS	Primary T cells from cord blood	blood
14	chr7:16263400-16264200	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr7:16263600-16263800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:16263800-16264200	Flanking Active TSS	Primary T cells from cord blood	blood
17	chr7:16263800-16264200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr7:16263800-16264200	Active TSS	Osteobl	bone
19	chr7:16264200-16264400	Enhancers	Primary T cells from cord blood	blood
20	chr7:16269800-16271200	ZNF genes & repeats	Liver	Liver
21	chr7:16270000-16271200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:16270200-16271200	ZNF genes & repeats	Fetal Lung	lung
23	chr7:16270400-16270600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:16270400-16270800	ZNF genes & repeats	Left Ventricle	heart
25	chr7:16270400-16272200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
26	chr7:16270400-16272200	ZNF genes & repeats	Ovary	ovary
27	chr7:16270400-16272200	ZNF genes & repeats	Psoas Muscle	Psoas
28	chr7:16270800-16273400	ZNF genes & repeats	K562	blood
29	chr7:16271200-16273200	Weak transcription	Fetal Lung	lung
30	chr7:16271600-16272200	ZNF genes & repeats	Liver	Liver
31	chr7:16272000-16272200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
32	chr7:16272200-16272800	Weak transcription	Ovary	ovary
33	chr7:16272200-16272800	Weak transcription	Psoas Muscle	Psoas
34	chr7:16272200-16276600	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr7:16272200-16276800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr7:16272800-16273000	Enhancers	Primary T cells from cord blood	blood
37	chr7:16273000-16274200	Weak transcription	Primary T cells from cord blood	blood
38	chr7:16273200-16273400	Enhancers	Fetal Lung	lung
39	chr7:16273400-16274200	Weak transcription	Fetal Lung	lung
40	chr7:16273400-16274200	Weak transcription	K562	blood
41	chr7:16274200-16274800	Enhancers	Primary T cells from cord blood	blood
42	chr7:16274200-16274800	Enhancers	NHEK	skin
43	chr7:16274200-16275000	Enhancers	Fetal Lung	lung
44	chr7:16274200-16275600	Enhancers	Fetal Heart	heart
45	chr7:16274200-16275600	Enhancers	K562	blood
46	chr7:16274400-16275200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr7:16275000-16304400	Weak transcription	Fetal Lung	lung
48	chr7:16275200-16275800	Enhancers	Fetal Brain Female	brain
49	chr7:16276400-16276800	Enhancers	Fetal Brain Male	brain
50	chr7:16276800-16277200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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