Variant report

Variant	nsv1045473
Chromosome Location	chr16:12625727-12636982
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:375)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12633181-12633355	K562	blood:	n/a	n/a
2	ATF1	chr16:12633157-12633742	K562	blood:	n/a	n/a
3	ATF1	chr16:12635640-12635845	K562	blood:	n/a	n/a
4	ATF2	chr16:12629438-12630541	GM12878	blood:	n/a	n/a
5	ATF2	chr16:12632809-12633811	GM12878	blood:	n/a	n/a
6	ATF2	chr16:12629393-12630582	GM12878	blood:	n/a	n/a
7	ATF2	chr16:12632602-12633937	GM12878	blood:	n/a	n/a
8	ATF3	chr16:12635622-12635902	K562	blood:	n/a	n/a
9	BACH1	chr16:12633143-12633457	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr16:12632981-12633517	GM12878	blood:	n/a	n/a
11	BATF	chr16:12632913-12633782	GM12878	blood:	n/a	n/a
12	BATF	chr16:12629811-12630325	GM12878	blood:	n/a	n/a
13	BATF	chr16:12629274-12630385	GM12878	blood:	n/a	n/a
14	BCL11A	chr16:12632989-12633622	GM12878	blood:	n/a	n/a
15	BCL11A	chr16:12633061-12633394	GM12878	blood:	n/a	n/a
16	BCL11A	chr16:12629549-12630405	GM12878	blood:	n/a	chr16:12629725-12629734
17	BCL11A	chr16:12629995-12630330	GM12878	blood:	n/a	n/a
18	BCL3	chr16:12625872-12626086	GM12878	blood:	n/a	n/a
19	BCL3	chr16:12632947-12633510	GM12878	blood:	n/a	n/a
20	BCL3	chr16:12625852-12626126	GM12878	blood:	n/a	n/a
21	BCL3	chr16:12629387-12630458	GM12878	blood:	n/a	chr16:12629725-12629734
22	BCL3	chr16:12629874-12630293	GM12878	blood:	n/a	n/a
23	BCL3	chr16:12633003-12633718	GM12878	blood:	n/a	n/a
24	BCLAF1	chr16:12632953-12633687	GM12878	blood:	n/a	n/a
25	BCLAF1	chr16:12629181-12630446	GM12878	blood:	n/a	chr16:12629725-12629734
26	BCLAF1	chr16:12629271-12630517	GM12878	blood:	n/a	chr16:12629725-12629734
27	BCLAF1	chr16:12632789-12633730	GM12878	blood:	n/a	n/a
28	BHLHE40	chr16:12632599-12632757	K562	blood:	n/a	n/a
29	BHLHE40	chr16:12632579-12633590	GM12878	blood:	n/a	n/a
30	BHLHE40	chr16:12629326-12630373	GM12878	blood:	n/a	n/a
31	BHLHE40	chr16:12635567-12635885	K562	blood:	n/a	n/a
32	CEBPB	chr16:12635568-12635927	HepG2	liver:	n/a	chr16:12635747-12635758 chr16:12635897-12635908
33	CEBPB	chr16:12629765-12630542	GM12878	blood:	n/a	n/a
34	CEBPB	chr16:12629933-12630195	GM12878	blood:	n/a	n/a
35	CEBPB	chr16:12633519-12633716	A549	lung:	n/a	n/a
36	CEBPB	chr16:12635585-12635860	A549	lung:	n/a	chr16:12635747-12635758
37	CEBPB	chr16:12625755-12626043	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:12635566-12635904	IMR90	lung:	n/a	chr16:12635747-12635758
39	CEBPB	chr16:12636781-12638818	GM12878	blood:	n/a	n/a
40	CEBPB	chr16:12635593-12635907	K562	blood:	n/a	chr16:12635747-12635758
41	CEBPB	chr16:12635656-12635804	K562	blood:	n/a	chr16:12635747-12635758
42	CHD1	chr16:12629561-12630498	GM12878	blood:	n/a	n/a
43	CHD1	chr16:12632487-12632686	GM12878	blood:	n/a	n/a
44	CHD2	chr16:12629384-12630402	GM12878	blood:	n/a	n/a
45	CHD2	chr16:12632957-12633550	GM12878	blood:	n/a	n/a
46	CHD2	chr16:12632703-12632754	GM12878	blood:	n/a	n/a
47	CREB1	chr16:12632589-12633865	GM12878	blood:	n/a	n/a
48	CREB1	chr16:12632906-12633829	GM12878	blood:	n/a	n/a
49	CREB1	chr16:12629382-12630453	GM12878	blood:	n/a	n/a
50	CTCF	chr16:12629600-12629750	GM12865	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12632861-12632911	ProgFib	skin:	n/a
2	chr16:12625807-12625857	H1-hESC	embryonic stem cell:	embryo
3	chr16:12632861-12632911	GM19239	blood:	n/a
4	chr16:12625807-12625857	NHBE	bronchial:	n/a
5	chr16:12625807-12625857	NB4	blood:	n/a
6	chr16:12632861-12632911	AG04450	lung:	fetal
7	chr16:12625807-12625857	HCPEpiC	choroid plexus:	n/a
8	chr16:12625807-12625857	ProgFib	skin:	n/a
9	chr16:12625807-12625857	NHDF-neo	bronchial:	n/a
10	chr16:12625807-12625857	HepG2	liver:	n/a
11	chr16:12625807-12625857	HIPEpiC	eye:	n/a
12	chr16:12632861-12632911	SK-N-SH	brain:	n/a
13	chr16:12632861-12632911	HRPEpiC	eye:	n/a
14	chr16:12632861-12632911	GM12892	blood:	n/a
15	chr16:12625807-12625857	T-47D	breast:	n/a
16	chr16:12625807-12625857	AG09309	skin:	n/a
17	chr16:12625807-12625857	PFSK-1	brain:	n/a
18	chr16:12625807-12625857	ECC-1	luminal epithelium:	n/a
19	chr16:12632861-12632911	GM06990	blood:	n/a
20	chr16:12625807-12625857	HCM	heart:	n/a
21	chr16:12625807-12625857	HAEpiC	amniotic membrane:	n/a
22	chr16:12632861-12632911	T-47D	breast:	n/a
23	chr16:12625807-12625857	NH-A	brain:	n/a
24	chr16:12632861-12632911	U87	brain:	n/a
25	chr16:12632861-12632911	MCF10A-Er-Src	breast:	n/a
26	chr16:12632861-12632911	HL-60	blood:	n/a
27	chr16:12632861-12632911	AG04449	skin:	fetal
28	chr16:12625807-12625857	RPTEC	kidney:	n/a
29	chr16:12632861-12632911	IMR90	lung:	fetal
30	chr16:12632861-12632911	PrEC	prostate:	n/a
31	chr16:12625807-12625857	HMEC	breast:	n/a
32	chr16:12632861-12632911	HRE	kidney:	n/a
33	chr16:12632861-12632911	HCT-116	colon:	n/a
34	chr16:12625807-12625857	AG10803	skin:	n/a
35	chr16:12632861-12632911	HIPEpiC	eye:	n/a
36	chr16:12632861-12632911	HepG2	liver:	n/a
37	chr16:12625807-12625857	CMK	blood:	n/a
38	chr16:12625807-12625857	HRPEpiC	eye:	n/a
39	chr16:12625807-12625857	IMR90	lung:	fetal
40	chr16:12625807-12625857	K562	blood:	n/a
41	chr16:12632861-12632911	RPTEC	kidney:	n/a
42	chr16:12632861-12632911	Hepatocyte	liver:	n/a
43	chr16:12625807-12625857	A549	lung:	n/a
44	chr16:12632861-12632911	HPAEpiC	pulmonary alveolar:	n/a
45	chr16:12632861-12632911	SK-N-MC	brain:	n/a
46	chr16:12625807-12625857	U87	brain:	n/a
47	chr16:12625807-12625857	Hela-S3	cervix:	n/a
48	chr16:12632861-12632911	HRCEpiC	kidney:	n/a
49	chr16:12632861-12632911	Hela-S3	cervix:	n/a
50	chr16:12625807-12625857	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:12633130..12635327-chr16:12640812..12643626,2	K562	blood:
2	chr16:12611118..12612757-chr16:12625721..12628602,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000260601	TF binding region
ENSG00000260601	CpG island

Extended variants
information (count: 1530 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189516469	chr16:12625735-12625736	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538595225	chr16:12625741-12625742	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552344495	chr16:12625758-12625759	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114976000	chr16:12625763-12625764	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537114461	chr16:12625781-12625782	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373067167	chr16:12625789-12625790	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557055090	chr16:12625790-12625791	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573653138	chr16:12625791-12625792	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181519563	chr16:12625807-12625808	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184654083	chr16:12625811-12625812	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189789776	chr16:12625829-12625830	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145387972	chr16:12625832-12625833	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368537710	chr16:12625836-12625837	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7195492	chr16:12625844-12625845	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs181439730	chr16:12625858-12625859	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534337786	chr16:12625900-12625901	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544292820	chr16:12625911-12625912	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560966951	chr16:12625918-12625919	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529670555	chr16:12625930-12625931	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186074778	chr16:12625955-12625956	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559937942	chr16:12625980-12625981	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572329620	chr16:12625988-12625989	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114088996	chr16:12625989-12625990	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74009121	chr16:12626007-12626008	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs569006941	chr16:12626009-12626010	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190603010	chr16:12626021-12626022	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs180874986	chr16:12626027-12626028	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186125631	chr16:12626073-12626074	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543633204	chr16:12626115-12626116	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190997475	chr16:12626116-12626117	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182832711	chr16:12626130-12626131	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559798328	chr16:12626135-12626136	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573192895	chr16:12626147-12626148	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187508328	chr16:12626148-12626149	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147692775	chr16:12626160-12626161	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191405024	chr16:12626162-12626163	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544826326	chr16:12626173-12626174	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530369647	chr16:12626175-12626176	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561503814	chr16:12626184-12626185	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574580918	chr16:12626186-12626187	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569244843	chr16:12626191-12626192	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182776326	chr16:12626228-12626229	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560077904	chr16:12626233-12626234	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77363973	chr16:12626235-12626236	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546032590	chr16:12626260-12626261	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188293136	chr16:12626271-12626272	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138248400	chr16:12626295-12626296	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142464425	chr16:12626311-12626312	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547980851	chr16:12626319-12626320	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192183153	chr16:12626337-12626338	Weak transcription Enhancers Strong transcription	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
Schizophrenia	23813976	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12603200-12626400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr16:12605800-12632200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr16:12606000-12632000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr16:12606200-12632400	Weak transcription	Right Atrium	heart
5	chr16:12607800-12626200	Weak transcription	Brain Germinal Matrix	brain
6	chr16:12608000-12632400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr16:12610000-12632400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr16:12610800-12632200	Weak transcription	Psoas Muscle	Psoas
9	chr16:12611600-12632400	Weak transcription	Left Ventricle	heart
10	chr16:12612400-12626600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr16:12612400-12626600	Weak transcription	Right Ventricle	heart
12	chr16:12612400-12632000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr16:12612600-12626400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr16:12613000-12670800	Weak transcription	Pancreas	Pancrea
15	chr16:12616000-12626600	Weak transcription	Thymus	Thymus
16	chr16:12617000-12626600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr16:12617400-12627000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr16:12618600-12626200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr16:12619000-12626000	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr16:12619000-12632200	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr16:12619800-12632000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr16:12620600-12630200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr16:12621000-12632400	Weak transcription	Adipose Nuclei	Adipose
24	chr16:12621600-12625800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr16:12621600-12628000	Weak transcription	GM12878-XiMat	blood
26	chr16:12622400-12625800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr16:12623600-12627200	Enhancers	Brain Hippocampus Middle	brain
28	chr16:12623800-12627000	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr16:12623800-12627400	Enhancers	Brain Substantia Nigra	brain
30	chr16:12624000-12631600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr16:12624000-12632000	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr16:12624000-12632400	Weak transcription	Aorta	Aorta
33	chr16:12624000-12632600	Weak transcription	Lung	lung
34	chr16:12624200-12625800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr16:12624200-12626600	Weak transcription	Primary T cells from cord blood	blood
36	chr16:12624200-12627000	Weak transcription	Primary B cells from peripheral blood	blood
37	chr16:12624800-12626000	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr16:12624800-12627200	Enhancers	Brain Cingulate Gyrus	brain
39	chr16:12625000-12626200	Enhancers	Spleen	Spleen
40	chr16:12625200-12626000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr16:12625400-12625800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr16:12625400-12625800	Enhancers	Gastric	stomach
43	chr16:12625400-12626000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr16:12625400-12626000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr16:12625400-12626200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr16:12625400-12626600	Weak transcription	Fetal Thymus	thymus
47	chr16:12625400-12626800	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr16:12625400-12627200	Enhancers	Brain Angular Gyrus	brain
49	chr16:12625400-12633400	Enhancers	Primary T cells fromperipheralblood	blood
50	chr16:12625600-12626000	Enhancers	A549	lung

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