Variant report

Variant	nsv984257
Chromosome Location	chr16:11968206-11992901
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr16:11968438-11968446	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr16:11971288-11971722	MCF-7	breast:	n/a	chr16:11971482-11971493 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971481-11971494
3	CEBPB	chr16:11971206-11971726	MCF-7	breast:	n/a	chr16:11971482-11971493 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971481-11971494
4	CEBPB	chr16:11987792-11987842	HepG2	liver:	n/a	n/a
5	CEBPB	chr16:11971301-11971632	A549	lung:	n/a	chr16:11971482-11971493 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971481-11971494
6	CEBPB	chr16:11971391-11971660	H1-hESC	embryonic stem cell:	n/a	chr16:11971482-11971493 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971481-11971494
7	CEBPB	chr16:11971285-11971768	A549	lung:	n/a	chr16:11971482-11971493 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971481-11971494
8	CEBPB	chr16:11971298-11971677	IMR90	lung:	n/a	chr16:11971482-11971493 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971481-11971494
9	CEBPB	chr16:11971290-11971676	Hela-S3	cervix:	n/a	chr16:11971482-11971493 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971481-11971494
10	CEBPB	chr16:11971309-11971668	HepG2	liver:	n/a	chr16:11971482-11971493 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971481-11971494
11	CEBPB	chr16:11971297-11971669	A549	lung:	n/a	chr16:11971482-11971493 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971481-11971494
12	CEBPB	chr16:11990626-11991065	IMR90	lung:	n/a	n/a
13	CEBPB	chr16:11971307-11971659	K562	blood:	n/a	chr16:11971482-11971493 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971483-11971492 chr16:11971481-11971494
14	CTCF	chr16:11974140-11974290	HRE	kidney:	n/a	n/a
15	CTCF	chr16:11974081-11974089	Medullo	brain:	n/a	n/a
16	CTCF	chr16:11974020-11974170	HCT-116	colon:	n/a	n/a
17	CTCF	chr16:11974020-11974170	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr16:11974000-11974150	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr16:11974020-11974170	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr16:11974020-11974170	NHEK	skin:	n/a	n/a
21	CTCF	chr16:11974105-11974183	Lung_OC	lung:	n/a	n/a
22	CTCF	chr16:11974000-11974150	GM12873	blood:	n/a	n/a
23	CTCF	chr16:11974000-11974150	HMEC	breast:	n/a	n/a
24	CTCF	chr16:11974093-11974136	GM12878	blood:	n/a	n/a
25	CTCF	chr16:11974060-11974210	HMEC	breast:	n/a	n/a
26	CTCF	chr16:11973096-11973195	GM20000	blood:	n/a	n/a
27	CTCF	chr16:11974080-11974230	MCF-7	breast:	n/a	n/a
28	CTCF	chr16:11974040-11974190	AG04450	lung:	n/a	n/a
29	CTCF	chr16:11974040-11974190	AG10803	skin:	n/a	n/a
30	CTCF	chr16:11973980-11974130	GM12874	blood:	n/a	n/a
31	CTCF	chr16:11974000-11974150	SAEC	small airway:	n/a	n/a
32	CTCF	chr16:11974050-11974187	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr16:11974080-11974230	GM12875	blood:	n/a	n/a
34	CTCF	chr16:11974020-11974170	A549	lung:	n/a	n/a
35	CTCF	chr16:11973960-11974110	HRE	kidney:	n/a	n/a
36	E2F4	chr16:11974099-11974275	MCF10A-Er-Src	breast:	n/a	n/a
37	EP300	chr16:11971341-11971644	Hela-S3	cervix:	n/a	n/a
38	FOS	chr16:11971321-11971644	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr16:11971321-11971641	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr16:11986633-11986941	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr16:11990674-11990991	MCF10A-Er-Src	breast:	n/a	chr16:11990852-11990860 chr16:11990853-11990864
42	FOS	chr16:11986733-11986960	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr16:11971321-11971656	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr16:11990611-11991028	HUVEC	blood vessel:	n/a	chr16:11990852-11990860 chr16:11990853-11990864
45	FOS	chr16:11990650-11990971	MCF10A-Er-Src	breast:	n/a	chr16:11990852-11990860 chr16:11990853-11990864
46	FOS	chr16:11971317-11971652	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr16:11990674-11991000	MCF10A-Er-Src	breast:	n/a	chr16:11990852-11990860 chr16:11990853-11990864
48	FOS	chr16:11990691-11990898	MCF10A-Er-Src	breast:	n/a	chr16:11990852-11990860 chr16:11990853-11990864
49	FOS	chr16:11986662-11986954	MCF10A-Er-Src	breast:	n/a	n/a
50	GATA3	chr16:11971297-11971653	T-47D	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:11768134..11770155-chr16:11969703..11971604,2	MCF-7	breast:
2	chr16:11986091..11989126-chr16:11998045..12000839,3	K562	blood:
3	chr16:11944038..11947076-chr16:11983498..11987330,3	MCF-7	breast:
4	chr16:11988100..11996073-chr16:12007143..12011577,10	MCF-7	breast:
5	chr16:11945202..11946733-chr16:11979732..11982221,2	MCF-7	breast:
6	chr16:11973175..11975559-chr16:11979030..11980935,2	MCF-7	breast:
7	chr16:11834739..11836576-chr16:11971624..11973137,2	MCF-7	breast:
8	chr16:11944290..11948249-chr16:11970756..11973644,3	MCF-7	breast:
9	chr16:11988764..11995180-chr16:12006980..12012068,9	MCF-7	breast:
10	chr16:11981260..11984239-chr16:11994473..11997426,2	K562	blood:
11	chr16:11990000..11991913-chr16:11997850..12000555,2	MCF-7	breast:
12	chr16:11968165..11970950-chr16:11974368..11976802,2	K562	blood:
13	chr16:11982694..11985676-chr16:12003356..12006033,2	MCF-7	breast:
14	chr16:11835919..11837744-chr16:11966699..11968629,2	MCF-7	breast:
15	chr16:11959980..11962642-chr16:11968005..11970163,2	K562	blood:
16	chr16:11958981..11960490-chr16:11981587..11984352,2	MCF-7	breast:
17	chr16:11985180..11986747-chr16:11988596..11990967,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-166B2.1.1-4	chr16:11988811-11989141	NONHSAT140603
2	lnc-RSL1D1-2	chr16:11974932-11976426	ENSG00000261560.1
3	lnc-TNFRSF17-2	chr16:11989346-11989468	ENSG00000263307.1
4	lnc-RP11-166B2.1.1-4	chr16:11984650-11984996	NONHSAT140603

Variant related genes	Relation type
GSPT1	TF binding region
ENSG00000261560	TF binding region
ENSG00000266163	chromatin interactions
ENSG00000260318	chromatin interactions
ENSG00000171490	chromatin interactions
ENSG00000103342	chromatin interactions
ENSG00000262420	chromatin interactions
ENSG00000263307	chromatin interactions
ENSG00000153066	chromatin interactions
ENSG00000261560	chromatin interactions

Extended variants
information (count: 1061 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1061 , 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	rs145565102	chr16:11968206-11968207	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs546259992	chr16:11968212-11968213	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs562897551	chr16:11968217-11968218	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs548202359	chr16:11968235-11968236	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs148868779	chr16:11968277-11968278	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs200991035	chr16:11968312-11968313	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs113140643	chr16:11968335-11968336	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs397971291	chr16:11968341-11968342	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs528326793	chr16:11968363-11968364	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs550862592	chr16:11968371-11968372	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs11075028	chr16:11968384-11968385	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs35932170	chr16:11968388-11968389	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs117215647	chr16:11968443-11968444	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs529861138	chr16:11968462-11968463	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs562189193	chr16:11968474-11968475	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs71383301	chr16:11968511-11968512	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546367833	chr16:11968553-11968554	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs28279	chr16:11968555-11968556	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs57628060	chr16:11968605-11968606	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs143296774	chr16:11968608-11968609	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191565837	chr16:11968611-11968612	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs148320608	chr16:11968631-11968632	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182539823	chr16:11968646-11968647	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537406571	chr16:11968690-11968691	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375873580	chr16:11968724-11968725	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555262974	chr16:11968771-11968772	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568635641	chr16:11968774-11968775	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs386789054	chr16:11968775-11968776	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs554397609	chr16:11968776-11968777	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145636669	chr16:11968777-11968778	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546321430	chr16:11968784-11968785	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs533468932	chr16:11968786-11968787	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs186500540	chr16:11968795-11968796	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541830358	chr16:11968804-11968805	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561264149	chr16:11968813-11968814	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs529923641	chr16:11968815-11968816	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569914408	chr16:11968816-11968817	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191438122	chr16:11968819-11968820	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs559915073	chr16:11968820-11968821	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs557097587	chr16:11968823-11968824	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552260210	chr16:11968838-11968839	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138498381	chr16:11968845-11968846	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531364132	chr16:11968858-11968859	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs74738468	chr16:11968863-11968864	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs190498151	chr16:11968864-11968865	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs534492776	chr16:11968865-11968866	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs554458954	chr16:11968871-11968872	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571065013	chr16:11968875-11968876	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs150685672	chr16:11968876-11968877	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555491709	chr16:11968879-11968880	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Breast cancer	21858162	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
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lujan-Fryns syndrom	21521776	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
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:11946200-11975600	Weak transcription	Aorta	Aorta
2	chr16:11946400-11969400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr16:11946400-11969400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr16:11946400-11969400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:11946400-11975600	Weak transcription	Esophagus	oesophagus
6	chr16:11946600-11969000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr16:11946600-11970400	Weak transcription	Right Atrium	heart
8	chr16:11947000-11969400	Weak transcription	Right Ventricle	heart
9	chr16:11947200-11968800	Weak transcription	Ovary	ovary
10	chr16:11948400-11969000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr16:11948600-11969000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr16:11948800-11969400	Weak transcription	Brain Angular Gyrus	brain
13	chr16:11948800-11970200	Weak transcription	Gastric	stomach
14	chr16:11958800-11969200	Weak transcription	Psoas Muscle	Psoas
15	chr16:11959400-11969400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr16:11960600-11969400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr16:11960600-11969600	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr16:11961200-11972200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr16:11961400-11975600	Weak transcription	Pancreas	Pancrea
20	chr16:11961600-11971600	Strong transcription	NHDF-Ad	bronchial
21	chr16:11961600-11986000	Weak transcription	Stomach Mucosa	stomach
22	chr16:11961800-11969400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr16:11961800-11972400	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr16:11961800-11991000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr16:11962000-11992200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr16:11962000-11994600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr16:11962200-11970200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr16:11962200-11992000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr16:11962400-11971800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr16:11962400-11972800	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr16:11962400-11982600	Strong transcription	Fetal Thymus	thymus
32	chr16:11962400-11984000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr16:11962400-11990800	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr16:11962400-11992000	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr16:11962400-11992200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr16:11962400-11992200	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr16:11962400-11992400	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr16:11962400-11995000	Strong transcription	Dnd41	blood
39	chr16:11962600-11971200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr16:11962600-11985600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr16:11962600-11990600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr16:11962600-11991800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr16:11962600-12004000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr16:11963000-11971000	Strong transcription	Hela-S3	cervix
45	chr16:11963200-11970800	Weak transcription	Brain Cingulate Gyrus	brain
46	chr16:11963400-11969400	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr16:11963400-11972600	Strong transcription	K562	blood
48	chr16:11963400-11975000	Weak transcription	Fetal Kidney	kidney
49	chr16:11963600-11968800	Weak transcription	NHLF	lung
50	chr16:11963800-11969400	Weak transcription	Brain Anterior Caudate	brain

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