Variant report

Variant	nsv1044772
Chromosome Location	chr16:12648266-12668751
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:461)
CpG islands
(count:671)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12667681-12668060	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:12664201-12664286	HepG2	liver:	n/a	n/a
3	ATF2	chr16:12666972-12667661	GM12878	blood:	n/a	n/a
4	ATF2	chr16:12666927-12667980	GM12878	blood:	n/a	n/a
5	BACH1	chr16:12667697-12667939	K562	blood:	n/a	n/a
6	BATF	chr16:12667208-12667587	GM12878	blood:	n/a	n/a
7	BCL3	chr16:12667035-12667697	GM12878	blood:	n/a	n/a
8	BCL3	chr16:12667189-12667642	GM12878	blood:	n/a	n/a
9	BCLAF1	chr16:12667037-12667943	GM12878	blood:	n/a	n/a
10	BCLAF1	chr16:12666973-12667572	GM12878	blood:	n/a	n/a
11	BHLHE40	chr16:12664073-12664400	HepG2	liver:	n/a	n/a
12	BHLHE40	chr16:12667748-12667970	K562	blood:	n/a	n/a
13	BHLHE40	chr16:12667237-12667896	GM12878	blood:	n/a	n/a
14	CEBPB	chr16:12662622-12662650	K562	blood:	n/a	n/a
15	CEBPB	chr16:12664077-12664393	HepG2	liver:	n/a	n/a
16	CEBPB	chr16:12667136-12667964	GM12878	blood:	n/a	n/a
17	CEBPB	chr16:12664070-12664394	HepG2	liver:	n/a	n/a
18	CEBPB	chr16:12653713-12653913	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr16:12653660-12653918	IMR90	lung:	n/a	n/a
20	CHD2	chr16:12667782-12667927	HepG2	liver:	n/a	n/a
21	CTCF	chr16:12667701-12667933	GM10266	blood:	n/a	n/a
22	CTCF	chr16:12667740-12667890	GM12872	blood:	n/a	n/a
23	CTCF	chr16:12667780-12667930	HMF	breast:	n/a	n/a
24	CTCF	chr16:12667740-12667890	HEK293	kidney:	n/a	n/a
25	CTCF	chr16:12667700-12667850	GM12875	blood:	n/a	n/a
26	CTCF	chr16:12667760-12667910	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr16:12652444-12652924	MCF-7	breast:	n/a	n/a
28	CTCF	chr16:12652600-12652750	K562	blood:	n/a	n/a
29	CTCF	chr16:12652604-12652785	MCF-7	breast:	n/a	n/a
30	CTCF	chr16:12652607-12652758	MCF-7	breast:	n/a	n/a
31	CTCF	chr16:12652540-12652690	GM12872	blood:	n/a	n/a
32	CTCF	chr16:12667740-12667890	GM12871	blood:	n/a	n/a
33	CTCF	chr16:12667780-12667930	GM12868	blood:	n/a	n/a
34	CTCF	chr16:12667800-12667950	NB4	blood:	n/a	n/a
35	CTCF	chr16:12652580-12652730	HCT-116	colon:	n/a	n/a
36	CTCF	chr16:12667703-12667948	A549	lung:	n/a	n/a
37	CTCF	chr16:12667740-12667890	RPTEC	kidney:	n/a	n/a
38	CTCF	chr16:12667760-12667910	AG10803	skin:	n/a	n/a
39	CTCF	chr16:12667740-12667890	Caco-2	colon:	n/a	n/a
40	CTCF	chr16:12667780-12667930	SAEC	small airway:	n/a	n/a
41	CTCF	chr16:12667720-12667870	GM12867	blood:	n/a	n/a
42	CTCF	chr16:12667481-12668276	HCT-116	colon:	n/a	n/a
43	CTCF	chr16:12667559-12668002	HCT-116	colon:	n/a	n/a
44	CTCF	chr16:12667701-12667940	ProgFib	skin:	n/a	n/a
45	CTCF	chr16:12667549-12668091	HepG2	liver:	n/a	n/a
46	CTCF	chr16:12667699-12667941	A549	lung:	n/a	n/a
47	CTCF	chr16:12667800-12667950	GM06990	blood:	n/a	n/a
48	CTCF	chr16:12652643-12652730	GM10248	blood:	n/a	n/a
49	CTCF	chr16:12667657-12667920	T-47D	breast:	n/a	n/a
50	CTCF	chr16:12667720-12667870	RPTEC	kidney:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12662581-12662631	HEEpiC	esophagus:	n/a
2	chr16:12662581-12662631	CMK	blood:	n/a
3	chr16:12659137-12659187	BJ	skin:	n/a
4	chr16:12662581-12662631	HRPEpiC	eye:	n/a
5	chr16:12667646-12667696	HRCEpiC	kidney:	n/a
6	chr16:12665018-12665068	PFSK-1	brain:	n/a
7	chr16:12662581-12662631	AG09309	skin:	n/a
8	chr16:12662474-12662524	NHDF-neo	bronchial:	n/a
9	chr16:12662659-12662709	NH-A	brain:	n/a
10	chr16:12656958-12657008	NB4	blood:	n/a
11	chr16:12657151-12657201	ECC-1	luminal epithelium:	n/a
12	chr16:12659137-12659187	HAEpiC	amniotic membrane:	n/a
13	chr16:12662581-12662631	HCPEpiC	choroid plexus:	n/a
14	chr16:12661268-12661318	BE2_C	brain:	n/a
15	chr16:12661268-12661318	Caco-2	colon:	n/a
16	chr16:12667646-12667696	GM12891	blood:	n/a
17	chr16:12657151-12657201	BJ	skin:	n/a
18	chr16:12662581-12662631	NB4	blood:	n/a
19	chr16:12667646-12667696	PANC-1	pancreas:	n/a
20	chr16:12662581-12662631	AoSMC	blood vessel:	n/a
21	chr16:12662474-12662524	GM12892	blood:	n/a
22	chr16:12665018-12665068	H1-hESC	embryonic stem cell:	embryo
23	chr16:12661268-12661318	GM12891	blood:	n/a
24	chr16:12656958-12657008	RPTEC	kidney:	n/a
25	chr16:12657151-12657201	HRCEpiC	kidney:	n/a
26	chr16:12659137-12659187	IMR90	lung:	fetal
27	chr16:12662374-12662424	HRCEpiC	kidney:	n/a
28	chr16:12661268-12661318	HNPCEpiC	eye:	n/a
29	chr16:12662581-12662631	HL-60	blood:	n/a
30	chr16:12662659-12662709	LNCaP	prostate:	n/a
31	chr16:12662474-12662524	AG04450	lung:	fetal
32	chr16:12662581-12662631	GM12891	blood:	n/a
33	chr16:12662374-12662424	ECC-1	luminal epithelium:	n/a
34	chr16:12661268-12661318	GM06990	blood:	n/a
35	chr16:12662659-12662709	GM12892	blood:	n/a
36	chr16:12659137-12659187	A549	lung:	n/a
37	chr16:12667646-12667696	ProgFib	skin:	n/a
38	chr16:12659137-12659187	HL-60	blood:	n/a
39	chr16:12665018-12665068	A549	lung:	n/a
40	chr16:12661268-12661318	AG10803	skin:	n/a
41	chr16:12667646-12667696	NT2-D1	testis:	n/a
42	chr16:12662374-12662424	Caco-2	colon:	n/a
43	chr16:12664318-12664368	Hela-S3	cervix:	n/a
44	chr16:12662659-12662709	CMK	blood:	n/a
45	chr16:12662659-12662709	NB4	blood:	n/a
46	chr16:12664318-12664368	T-47D	breast:	n/a
47	chr16:12665018-12665068	RPTEC	kidney:	n/a
48	chr16:12667646-12667696	HRPEpiC	eye:	n/a
49	chr16:12661268-12661318	MCF10A-Er-Src	breast:	n/a
50	chr16:12662581-12662631	HMEC	breast:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:12667441..12668160-chr16:12908986..12909620,2	K562	blood:
2	chr16:12646912..12648633-chr16:12652435..12654729,2	K562	blood:
3	chr16:12667763..12668530-chr16:12912908..12913815,2	MCF-7	breast:
4	chr16:12667311..12668307-chr16:12912660..12913925,10	K562	blood:
5	chr16:12656706..12658781-chr16:12659071..12661791,2	MCF-7	breast:
6	chr16:12651809..12653725-chr16:12657374..12659013,2	MCF-7	breast:
7	chr16:12667422..12668391-chr16:12912804..12913870,6	MCF-7	breast:
8	chr16:12548883..12549752-chr16:12667238..12668263,4	MCF-7	breast:
9	chr16:12666208..12667949-chr16:12909884..12912499,2	K562	blood:
10	chr16:12667303..12668256-chr16:12994641..12995560,2	MCF-7	breast:
11	chr16:12664367..12666728-chr16:12670658..12673027,2	K562	blood:
12	chr16:12667239..12668915-chr16:12896290..12899009,2	MCF-7	breast:
13	chr16:12667431..12668234-chr16:12930367..12931210,2	MCF-7	breast:
14	chr16:12651809..12653725-chr16:12657374..12659013,2	MCF-7	breast:
15	chr16:12656706..12658781-chr16:12659071..12661791,2	MCF-7	breast:
16	chr16:12646912..12648633-chr16:12652435..12654729,2	K562	blood:
17	chr16:12652319..12653186-chr16:12913152..12913807,2	MCF-7	breast:
18	chr16:12667378..12668264-chr16:12909027..12909976,6	MCF-7	breast:
19	chr16:12434411..12435246-chr16:12667446..12668002,2	MCF-7	breast:
20	chr16:12667518..12668062-chr16:12712002..12712507,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPPED1-3	chr16:12650210-12650396	ENSG00000259876.1
2	lnc-CPPED1-2	chr16:12654613-12655003	ENSG00000259899.1
3	lnc-CPPED1-3	chr16:12651176-12651551	ENSG00000259876.1

No data

Variant related genes	Relation type
ENSG00000259876	TF binding region
ENSG00000259876	CpG island
ENSG00000103381	chromatin interactions
ENSG00000237515	chromatin interactions

Extended variants
information (count: 3518 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3518 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2561039	chr16:12648266-12648267	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76216803	chr16:12648272-12648273	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562787810	chr16:12648278-12648279	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76143244	chr16:12648279-12648280	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554624042	chr16:12648298-12648299	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112592278	chr16:12648305-12648306	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548917041	chr16:12648315-12648316	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141288482	chr16:12648318-12648319	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534368750	chr16:12648321-12648322	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548044519	chr16:12648323-12648324	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187284775	chr16:12648343-12648344	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs5815694	chr16:12648347-12648348	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374662477	chr16:12648348-12648349	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538314956	chr16:12648349-12648350	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539207649	chr16:12648352-12648353	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77204878	chr16:12648360-12648361	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs117115998	chr16:12648361-12648362	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568484325	chr16:12648364-12648365	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535328782	chr16:12648371-12648372	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371808263	chr16:12648382-12648383	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192084390	chr16:12648389-12648390	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147009890	chr16:12648390-12648391	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7191878	chr16:12648391-12648392	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs377708866	chr16:12648396-12648397	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76862817	chr16:12648401-12648402	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545984363	chr16:12648405-12648406	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562858908	chr16:12648406-12648407	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138223538	chr16:12648409-12648410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548631950	chr16:12648413-12648414	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562353938	chr16:12648416-12648417	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528032624	chr16:12648427-12648428	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547968974	chr16:12648429-12648430	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143380738	chr16:12648432-12648433	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76323542	chr16:12648434-12648435	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545659159	chr16:12648438-12648439	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182863372	chr16:12648440-12648441	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565167426	chr16:12648449-12648450	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186061030	chr16:12648450-12648451	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139490176	chr16:12648451-12648452	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs3848243	chr16:12648455-12648456	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs7190533	chr16:12648460-12648461	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs534646853	chr16:12648493-12648494	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149273584	chr16:12648497-12648498	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190524267	chr16:12648503-12648504	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577770567	chr16:12648505-12648506	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112473998	chr16:12648507-12648508	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546252626	chr16:12648523-12648524	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565397232	chr16:12648526-12648527	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373123519	chr16:12648528-12648529	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79862059	chr16:12648532-12648533	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	17603634	CNVD
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	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	22102821	CNVD
Autism	22495311	CNVD
idiopathic generalized epilepsy	19843651	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Intellectual disability	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	19786961	CNVD
Mental retardation	19786961	CNVD
Schizophrenia	19786961	CNVD
Mental retardation	19951919	CNVD
Autism	18791038	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Malignant germ cell tumour	17285132	CNVD
Autism	17480035	CNVD
Schizophrenia	19955444	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	17847001	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12613000-12670800	Weak transcription	Pancreas	Pancrea
2	chr16:12632800-12663800	Weak transcription	Aorta	Aorta
3	chr16:12633400-12654400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr16:12639400-12659000	Weak transcription	Lung	lung
5	chr16:12641200-12667000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr16:12642000-12662200	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr16:12642200-12655000	Weak transcription	Spleen	Spleen
8	chr16:12642400-12653000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr16:12643000-12659200	Weak transcription	Placenta	Placenta
10	chr16:12643200-12653000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr16:12645200-12661600	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr16:12645600-12652200	Weak transcription	Primary B cells from cord blood	blood
13	chr16:12646000-12648800	Enhancers	Esophagus	oesophagus
14	chr16:12646000-12655400	Weak transcription	Gastric	stomach
15	chr16:12646000-12659000	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr16:12646000-12661000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr16:12646200-12649600	Weak transcription	Right Atrium	heart
18	chr16:12646200-12651000	Weak transcription	GM12878-XiMat	blood
19	chr16:12646200-12654800	Weak transcription	Primary T cells from cord blood	blood
20	chr16:12646200-12659800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr16:12646200-12660000	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr16:12646400-12659400	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr16:12646400-12660800	Weak transcription	Thymus	Thymus
24	chr16:12646600-12648400	Enhancers	Brain Substantia Nigra	brain
25	chr16:12646600-12649200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr16:12647400-12650000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr16:12647400-12650200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr16:12647400-12651000	Weak transcription	Brain Angular Gyrus	brain
29	chr16:12647400-12651200	Weak transcription	Brain Anterior Caudate	brain
30	chr16:12647400-12651400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr16:12647400-12651600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr16:12647400-12658800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr16:12647400-12662200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr16:12647400-12665200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr16:12647600-12651000	Weak transcription	Brain Hippocampus Middle	brain
36	chr16:12647600-12661600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr16:12648000-12653000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr16:12648000-12662200	Weak transcription	Fetal Stomach	stomach
39	chr16:12648200-12648400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr16:12648200-12649800	Strong transcription	Primary B cells from peripheral blood	blood
41	chr16:12648200-12651400	Weak transcription	Brain Cingulate Gyrus	brain
42	chr16:12648400-12649200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr16:12648400-12651200	Weak transcription	Brain Substantia Nigra	brain
44	chr16:12648400-12668800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr16:12648800-12659200	Weak transcription	Esophagus	oesophagus
46	chr16:12649000-12658600	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr16:12649200-12649800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr16:12649200-12651000	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr16:12649600-12650600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr16:12649800-12650200	Weak transcription	Primary B cells from peripheral blood	blood

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