Variant report

Variant	nsv905755
Chromosome Location	chr16:31559220-31634221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:152)
CpG islands
(count:1039)
Chromatin interactive
region (count:7)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:152 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:31593151-31593199	K562	blood:	n/a	n/a
2	BACH1	chr16:31562517-31562553	K562	blood:	n/a	n/a
3	CBX3	chr16:31588768-31589075	K562	blood:	n/a	n/a
4	CBX3	chr16:31588835-31589018	K562	blood:	n/a	n/a
5	CEBPB	chr16:31620908-31621218	HepG2	liver:	n/a	chr16:31621045-31621056
6	CEBPB	chr16:31620971-31621116	IMR90	lung:	n/a	chr16:31621045-31621056
7	CEBPB	chr16:31591338-31591399	HepG2	liver:	n/a	chr16:31591372-31591383
8	CEBPB	chr16:31620982-31621195	A549	lung:	n/a	chr16:31621045-31621056
9	CTCF	chr16:31591760-31591910	HepG2	liver:	n/a	n/a
10	CTCF	chr16:31580280-31580430	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr16:31591440-31591590	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr16:31580254-31580404	K562	blood:	n/a	n/a
13	CTCF	chr16:31607297-31607367	Gliobla	brain:	n/a	n/a
14	CTCF	chr16:31580234-31580418	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr16:31591380-31591530	K562	blood:	n/a	n/a
16	CTCF	chr16:31580275-31580293	Fibrobl	skin:	n/a	n/a
17	CTCF	chr16:31580194-31580418	K562	blood:	n/a	n/a
18	CTCF	chr16:31591440-31591590	HEK293	kidney:	n/a	n/a
19	CTCF	chr16:31591521-31591601	HepG2	liver:	n/a	n/a
20	CTCF	chr16:31631227-31631322	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr16:31591460-31591610	GM12873	blood:	n/a	n/a
22	CTCF	chr16:31591537-31591604	GM12891	blood:	n/a	n/a
23	CTCF	chr16:31580259-31580390	ProgFib	skin:	n/a	n/a
24	CTCF	chr16:31567380-31567530	MCF-7	breast:	n/a	n/a
25	CTCF	chr16:31580183-31580504	K562	blood:	n/a	n/a
26	CTCF	chr16:31600410-31600442	GM20000	blood:	n/a	n/a
27	CTCF	chr16:31603780-31603930	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr16:31591521-31591524	GM12892	blood:	n/a	n/a
29	CTCF	chr16:31600140-31600290	HepG2	liver:	n/a	n/a
30	CTCF	chr16:31580220-31580370	AG04449	skin:	n/a	n/a
31	CTCF	chr16:31591505-31591579	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr16:31591460-31591610	HepG2	liver:	n/a	n/a
33	CTCF	chr16:31580246-31580387	NHEK	skin:	n/a	n/a
34	CTCF	chr16:31600080-31600230	HEK293	kidney:	n/a	n/a
35	CTCF	chr16:31600446-31600451	GM20000	blood:	n/a	n/a
36	CTCF	chr16:31580200-31580350	K562	blood:	n/a	n/a
37	CTCF	chr16:31600528-31600591	Fibrobl	skin:	n/a	n/a
38	CTCF	chr16:31591460-31591610	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr16:31580187-31580453	K562	blood:	n/a	n/a
40	CTCF	chr16:31580261-31580402	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr16:31580240-31580390	HRE	kidney:	n/a	n/a
42	CTCF	chr16:31591480-31591642	HepG2	liver:	n/a	n/a
43	CTCF	chr16:31591545-31591564	A549	lung:	n/a	n/a
44	CTCF	chr16:31591526-31591567	GM12892	blood:	n/a	n/a
45	CTCF	chr16:31591516-31591567	MCF-7	breast:	n/a	n/a
46	CTCF	chr16:31580220-31580370	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr16:31580248-31580403	Lung_OC	lung:	n/a	n/a
48	CTCF	chr16:31580281-31580383	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr16:31580242-31580402	IMR90	lung:	n/a	n/a
50	CTCF	chr16:31570248-31570297	Lung_OC	lung:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31584046-31584096	NHDF-neo	bronchial:	n/a
2	chr16:31580424-31580474	HRCEpiC	kidney:	n/a
3	chr16:31584046-31584096	NHDF-neo	bronchial:	n/a
4	chr16:31580424-31580474	HRCEpiC	kidney:	n/a
5	chr16:31581309-31581359	ECC-1	luminal epithelium:	n/a
6	chr16:31580424-31580474	HIPEpiC	eye:	n/a
7	chr16:31579805-31579855	A549	lung:	n/a
8	chr16:31580150-31580200	AG04449	skin:	fetal
9	chr16:31580889-31580939	HIPEpiC	eye:	n/a
10	chr16:31579647-31579697	ECC-1	luminal epithelium:	n/a
11	chr16:31580889-31580939	HRPEpiC	eye:	n/a
12	chr16:31580153-31580203	K562	blood:	n/a
13	chr16:31580424-31580474	BJ	skin:	n/a
14	chr16:31580989-31581039	BJ	skin:	n/a
15	chr16:31580964-31581014	AG04450	lung:	fetal
16	chr16:31579805-31579855	GM12878	blood:	n/a
17	chr16:31584046-31584096	K562	blood:	n/a
18	chr16:31584046-31584096	SAEC	small airway:	n/a
19	chr16:31579805-31579855	HMEC	breast:	n/a
20	chr16:31580424-31580474	HEEpiC	esophagus:	n/a
21	chr16:31584046-31584096	U87	brain:	n/a
22	chr16:31579805-31579855	H1-hESC	embryonic stem cell:	embryo
23	chr16:31580153-31580203	AG09319	gingival:	n/a
24	chr16:31581268-31581318	LNCaP	prostate:	n/a
25	chr16:31580889-31580939	HNPCEpiC	eye:	n/a
26	chr16:31581150-31581200	SK-N-SH	brain:	n/a
27	chr16:31579805-31579855	HCM	heart:	n/a
28	chr16:31580889-31580939	AG10803	skin:	n/a
29	chr16:31580989-31581039	AG10803	skin:	n/a
30	chr16:31580964-31581014	PrEC	prostate:	n/a
31	chr16:31580989-31581039	HRPEpiC	eye:	n/a
32	chr16:31580424-31580474	T-47D	breast:	n/a
33	chr16:31580424-31580474	MCF10A-Er-Src	breast:	n/a
34	chr16:31580590-31580640	HEEpiC	esophagus:	n/a
35	chr16:31580153-31580203	Hela-S3	cervix:	n/a
36	chr16:31581150-31581200	GM12891	blood:	n/a
37	chr16:31576872-31576922	T-47D	breast:	n/a
38	chr16:31579647-31579697	HMEC	breast:	n/a
39	chr16:31584046-31584096	HAEpiC	amniotic membrane:	n/a
40	chr16:31580590-31580640	NH-A	brain:	n/a
41	chr16:31581309-31581359	HPAEpiC	pulmonary alveolar:	n/a
42	chr16:31581309-31581359	GM19239	blood:	n/a
43	chr16:31576872-31576922	HepG2	liver:	n/a
44	chr16:31579805-31579855	HAEpiC	amniotic membrane:	n/a
45	chr16:31580299-31580349	HCPEpiC	choroid plexus:	n/a
46	chr16:31580424-31580474	NHBE	bronchial:	n/a
47	chr16:31576339-31576389	GM06990	blood:	n/a
48	chr16:31580150-31580200	H1-hESC	embryonic stem cell:	embryo
49	chr16:31581150-31581200	Jurkat	blood:	n/a
50	chr16:31580964-31581014	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:31566968..31568774-chr16:31592560..31594234,2	MCF-7	breast:
2	chr16:31556967..31559890-chr16:31567945..31570238,2	K562	blood:
3	chr16:31519671..31522254-chr16:31566727..31568830,2	MCF-7	breast:
4	chr16:31629167..31631052-chr16:31633702..31636647,2	K562	blood:
5	chr16:31563997..31565923-chr16:31567034..31569130,2	K562	blood:
6	chr16:31566968..31568774-chr16:31592560..31594234,2	MCF-7	breast:
7	chr16:31629167..31631052-chr16:31633702..31636647,2	K562	blood:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C16orf58-6	chr16:31575246-31575322	NONHSAT141936
2	lnc-AHSP-3	chr16:31625243-31625276	NONHSAT141942
3	lnc-C16orf58-6	chr16:31575929-31576029	NONHSAT141936
4	lnc-C16orf58-6	chr16:31575924-31576104	NONHSAT141935
5	lnc-C16orf58-3	chr16:31560464-31560608	ENSG00000261475.2
6	lnc-C16orf58-3	chr16:31560406-31560608	NONHSAT141932
7	lnc-C16orf58-6	chr16:31579088-31580845	NONHSAT141938
8	lnc-C16orf58-6	chr16:31575556-31575606	NONHSAT141935
9	lnc-AHSP-3	chr16:31624712-31624816	NONHSAT141942
10	lnc-C16orf58-6	chr16:31575246-31575322	NONHSAT141935
11	lnc-AHSP-3	chr16:31625713-31626173	NONHSAT141942
12	lnc-C16orf58-6	chr16:31574154-31574955	NONHSAT141934
13	lnc-C16orf58-6	chr16:31575246-31575322	NONHSAT141934
14	lnc-C16orf58-6	chr16:31574506-31574955	NONHSAT141936
15	lnc-AHSP-2	chr16:31565426-31566233	NONHSAT141933
16	lnc-C16orf58-6	chr16:31579707-31580796	NONHSAT141939
17	lnc-AHSP-3	chr16:31624492-31624614	NONHSAT141942
18	lnc-AHSP-4	chr16:31628780-31629709	expReg_chr16_4904_+
19	lnc-C16orf58-3	chr16:31564466-31564870	NONHSAT141929
20	lnc-C16orf58-6	chr16:31574403-31574920	NONHSAT141935
21	lnc-C16orf58-3	chr16:31564466-31564888	ENSG00000261475.2
22	lnc-C16orf58-7	chr16:31612914-31614852	NONHSAT141940
23	lnc-C16orf58-6	chr16:31575929-31576029	NONHSAT141934
24	lnc-C16orf58-6	chr16:31578695-31579197	NONHSAT141937
25	lnc-C16orf58-6	chr16:31602915-31602937	NONHSAT141934
26	lnc-C16orf58-6	chr16:31575897-31576029	NONHSAT141937
27	lnc-AHSP-3	chr16:31624494-31624840	NONHSAT141941
28	lnc-C16orf58-3	chr16:31564466-31564870	NONHSAT141932
29	lnc-C16orf58-6	chr16:31578695-31579037	NONHSAT141936
30	lnc-AHSP-3	chr16:31623102-31623212	NONHSAT141941
31	lnc-AHSP-3	chr16:31624171-31624294	NONHSAT141941

No data

Variant related genes	Relation type
ENSG00000261648	TF binding region
ZNF720P1	TF binding region
ENSG00000261741	TF binding region
VN1R65P	TF binding region
ENSG00000261475	TF binding region
YBX3P1	TF binding region
ENSG00000261648	CpG island
ZNF720P1	CpG island
ENSG00000261741	CpG island
VN1R65P	CpG island
ENSG00000261475	CpG island
YBX3P1	CpG island
ENSG00000260883	chromatin interactions
ENSG00000140688	chromatin interactions
ENSG00000261475	chromatin interactions
ENSG00000260625	chromatin interactions
ENSG00000213547	chromatin interactions
ENSG00000261648	chromatin interactions

Extended variants
information (count: 977 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4564590	chr16:31559220-31559221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs201162680	chr16:31559303-31559304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76603902	chr16:31559341-31559342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564143315	chr16:31559440-31559441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146416151	chr16:31559471-31559472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12596058	chr16:31559610-31559611	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs80055794	chr16:31559632-31559633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562884772	chr16:31559650-31559651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529874325	chr16:31559668-31559669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530245606	chr16:31559920-31559921	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs182137169	chr16:31560020-31560021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548385780	chr16:31560027-31560028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74747034	chr16:31560037-31560038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528253202	chr16:31560070-31560071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546873356	chr16:31560138-31560139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187096251	chr16:31560141-31560142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73540269	chr16:31560145-31560146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs550342731	chr16:31560151-31560152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568493941	chr16:31560203-31560204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191532747	chr16:31560218-31560219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554235380	chr16:31560227-31560228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111949046	chr16:31560260-31560261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185200692	chr16:31560274-31560275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534086355	chr16:31560337-31560338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77170379	chr16:31560405-31560406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569831192	chr16:31560425-31560426	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs544866560	chr16:31560432-31560433	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs140730287	chr16:31560455-31560456	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs574875305	chr16:31560462-31560463	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs369106425	chr16:31560469-31560470	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs370298685	chr16:31560506-31560507	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs541957512	chr16:31560523-31560524	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs560522334	chr16:31560575-31560576	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs4423435	chr16:31560603-31560604	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs4325581	chr16:31560674-31560675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145519410	chr16:31560796-31560797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74015561	chr16:31560836-31560837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs550850532	chr16:31560871-31560872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369759302	chr16:31561027-31561028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190043738	chr16:31561032-31561033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4369688	chr16:31561056-31561057	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs552823426	chr16:31561064-31561065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574499652	chr16:31561117-31561118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115513046	chr16:31561128-31561129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113656260	chr16:31561159-31561160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377432362	chr16:31561197-31561198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs59050904	chr16:31561244-31561245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs148969413	chr16:31561266-31561267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147088035	chr16:31561280-31561281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567254799	chr16:31561283-31561284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
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
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Sezary syndrome	18413736	CNVD
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31556200-31561600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:31561600-31562000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:31564400-31564600	ZNF genes & repeats	Spleen	Spleen
4	chr16:31568200-31568600	Flanking Active TSS	K562	blood
5	chr16:31568600-31568800	Active TSS	K562	blood
6	chr16:31572800-31573200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr16:31572800-31573400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr16:31573200-31579800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr16:31574400-31574600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr16:31579600-31580000	Enhancers	Gastric	stomach
11	chr16:31579600-31580400	ZNF genes & repeats	Lung	lung
12	chr16:31579600-31581000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
13	chr16:31579600-31581000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
14	chr16:31579600-31581400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
15	chr16:31579800-31580000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr16:31579800-31580000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr16:31579800-31580000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr16:31579800-31580000	Enhancers	Pancreas	Pancrea
19	chr16:31579800-31580200	Bivalent/Poised TSS	Brain Anterior Caudate	brain
20	chr16:31579800-31581000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
21	chr16:31579800-31581000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
22	chr16:31579800-31581200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
23	chr16:31579800-31581400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
24	chr16:31579800-31581400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
25	chr16:31580000-31580200	Enhancers	Primary hematopoietic stem cells	blood
26	chr16:31580000-31580200	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr16:31580000-31580200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
28	chr16:31580000-31580200	Bivalent Enhancer	Fetal Stomach	stomach
29	chr16:31580000-31580200	Active TSS	Rectal Smooth Muscle	rectum
30	chr16:31580000-31580200	Active TSS	Right Atrium	heart
31	chr16:31580000-31580200	Active TSS	Right Ventricle	heart
32	chr16:31580000-31580200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
33	chr16:31580000-31580200	Bivalent Enhancer	Stomach Mucosa	stomach
34	chr16:31580000-31580200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
35	chr16:31580000-31580400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr16:31580000-31580400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
37	chr16:31580000-31580400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
38	chr16:31580000-31580400	Flanking Active TSS	Gastric	stomach
39	chr16:31580000-31580400	Flanking Active TSS	Pancreas	Pancrea
40	chr16:31580000-31580400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
41	chr16:31580000-31580600	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
42	chr16:31580000-31580600	Bivalent Enhancer	Fetal Heart	heart
43	chr16:31580000-31580600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
44	chr16:31580000-31580600	Active TSS	Rectal Mucosa Donor 29	rectum
45	chr16:31580000-31580800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr16:31580000-31580800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr16:31580000-31580800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr16:31580000-31580800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr16:31580000-31580800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
50	chr16:31580000-31580800	Bivalent/Poised TSS	Brain Substantia Nigra	brain

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