Variant report

Variant	nsv1040887
Chromosome Location	chr16:12632918-12650247
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:525)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:525 , 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	chr16:12633181-12633355	K562	blood:	n/a	n/a
2	ARID3A	chr16:12637659-12638979	HepG2	liver:	n/a	n/a
3	ATF1	chr16:12635640-12635845	K562	blood:	n/a	n/a
4	ATF1	chr16:12633157-12633742	K562	blood:	n/a	n/a
5	ATF2	chr16:12639568-12640202	GM12878	blood:	n/a	n/a
6	ATF2	chr16:12642072-12642853	GM12878	blood:	n/a	n/a
7	ATF2	chr16:12637132-12637535	GM12878	blood:	n/a	n/a
8	ATF2	chr16:12637025-12638683	GM12878	blood:	n/a	n/a
9	ATF2	chr16:12637898-12638419	GM12878	blood:	n/a	n/a
10	ATF2	chr16:12640769-12641712	GM12878	blood:	n/a	n/a
11	ATF2	chr16:12632602-12633937	GM12878	blood:	n/a	n/a
12	ATF2	chr16:12642244-12642881	GM12878	blood:	n/a	n/a
13	ATF2	chr16:12632809-12633811	GM12878	blood:	n/a	n/a
14	ATF2	chr16:12640623-12641853	GM12878	blood:	n/a	n/a
15	ATF2	chr16:12639659-12640191	GM12878	blood:	n/a	n/a
16	ATF3	chr16:12635622-12635902	K562	blood:	n/a	n/a
17	BACH1	chr16:12633143-12633457	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr16:12641144-12641522	GM12878	blood:	n/a	n/a
19	BATF	chr16:12632981-12633517	GM12878	blood:	n/a	n/a
20	BATF	chr16:12632913-12633782	GM12878	blood:	n/a	n/a
21	BATF	chr16:12637164-12637545	GM12878	blood:	n/a	n/a
22	BATF	chr16:12637100-12637603	GM12878	blood:	n/a	n/a
23	BATF	chr16:12642081-12642829	GM12878	blood:	n/a	n/a
24	BATF	chr16:12637743-12638321	GM12878	blood:	n/a	chr16:12637886-12637896
25	BATF	chr16:12640856-12641664	GM12878	blood:	n/a	n/a
26	BATF	chr16:12642156-12642469	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:12637150-12637604	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:12632989-12633622	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:12642225-12642824	GM12878	blood:	n/a	chr16:12642696-12642705
30	BCL11A	chr16:12641124-12641591	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:12633061-12633394	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:12637890-12638396	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:12637166-12637556	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:12641066-12641666	GM12878	blood:	n/a	n/a
35	BCL3	chr16:12642227-12642860	GM12878	blood:	n/a	chr16:12642696-12642705
36	BCL3	chr16:12637811-12638327	GM12878	blood:	n/a	n/a
37	BCL3	chr16:12633003-12633718	GM12878	blood:	n/a	n/a
38	BCL3	chr16:12641071-12641581	GM12878	blood:	n/a	n/a
39	BCL3	chr16:12641073-12641684	GM12878	blood:	n/a	n/a
40	BCL3	chr16:12632947-12633510	GM12878	blood:	n/a	n/a
41	BCL3	chr16:12637165-12637549	GM12878	blood:	n/a	n/a
42	BCLAF1	chr16:12637031-12637643	GM12878	blood:	n/a	n/a
43	BCLAF1	chr16:12640983-12641815	GM12878	blood:	n/a	n/a
44	BCLAF1	chr16:12637158-12638446	GM12878	blood:	n/a	n/a
45	BCLAF1	chr16:12640683-12641726	GM12878	blood:	n/a	n/a
46	BCLAF1	chr16:12637669-12638335	GM12878	blood:	n/a	n/a
47	BCLAF1	chr16:12632789-12633730	GM12878	blood:	n/a	n/a
48	BCLAF1	chr16:12632953-12633687	GM12878	blood:	n/a	n/a
49	BHLHE40	chr16:12639724-12639965	GM12878	blood:	n/a	n/a
50	BHLHE40	chr16:12637849-12638304	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12637499-12637549	NH-A	brain:	n/a
2	chr16:12637499-12637549	AG04449	skin:	fetal
3	chr16:12637499-12637549	NB4	blood:	n/a
4	chr16:12637499-12637549	HIPEpiC	eye:	n/a
5	chr16:12637499-12637549	SKMC	muscle:	n/a
6	chr16:12637499-12637549	HCPEpiC	choroid plexus:	n/a
7	chr16:12637499-12637549	HMEC	breast:	n/a
8	chr16:12637499-12637549	AoSMC	blood vessel:	n/a
9	chr16:12637499-12637549	NHBE	bronchial:	n/a
10	chr16:12637499-12637549	HNPCEpiC	eye:	n/a
11	chr16:12637499-12637549	HAEpiC	amniotic membrane:	n/a
12	chr16:12637499-12637549	HUVEC	blood vessel:	n/a
13	chr16:12637499-12637549	ECC-1	luminal epithelium:	n/a
14	chr16:12637499-12637549	HEK293	kidney:	embryo
15	chr16:12637499-12637549	GM06990	blood:	n/a
16	chr16:12637499-12637549	U87	brain:	n/a
17	chr16:12637499-12637549	MCF-7	breast:	n/a
18	chr16:12637499-12637549	AG10803	skin:	n/a
19	chr16:12637499-12637549	K562	blood:	n/a
20	chr16:12637499-12637549	HL-60	blood:	n/a
21	chr16:12637499-12637549	HCM	heart:	n/a
22	chr16:12637499-12637549	AG09319	gingival:	n/a
23	chr16:12637499-12637549	T-47D	breast:	n/a
24	chr16:12637499-12637549	GM19239	blood:	n/a
25	chr16:12637499-12637549	Jurkat	blood:	n/a
26	chr16:12637499-12637549	HPAEpiC	pulmonary alveolar:	n/a
27	chr16:12637499-12637549	HepG2	liver:	n/a
28	chr16:12637499-12637549	Hela-S3	cervix:	n/a
29	chr16:12637499-12637549	LNCaP	prostate:	n/a
30	chr16:12637499-12637549	GM12892	blood:	n/a
31	chr16:12637499-12637549	HEEpiC	esophagus:	n/a
32	chr16:12637499-12637549	RPTEC	kidney:	n/a
33	chr16:12637499-12637549	CMK	blood:	n/a
34	chr16:12637499-12637549	HRPEpiC	eye:	n/a
35	chr16:12637499-12637549	HCT-116	colon:	n/a
36	chr16:12637499-12637549	BE2_C	brain:	n/a
37	chr16:12637499-12637549	ovcar-3	ovarian:	n/a
38	chr16:12637499-12637549	H1-hESC	embryonic stem cell:	embryo
39	chr16:12637499-12637549	PANC-1	pancreas:	n/a
40	chr16:12637499-12637549	ProgFib	skin:	n/a
41	chr16:12637499-12637549	PrEC	prostate:	n/a
42	chr16:12637499-12637549	IMR90	lung:	fetal
43	chr16:12637499-12637549	SK-N-MC	brain:	n/a
44	chr16:12637499-12637549	BJ	skin:	n/a
45	chr16:12637499-12637549	Hepatocyte	liver:	n/a
46	chr16:12637499-12637549	HCF	heart:	n/a
47	chr16:12637499-12637549	SAEC	small airway:	n/a
48	chr16:12637499-12637549	GM12891	blood:	n/a
49	chr16:12637499-12637549	HRE	kidney:	n/a
50	chr16:12637499-12637549	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:12633130..12635327-chr16:12640812..12643626,2	K562	blood:
2	chr16:12646912..12648633-chr16:12652435..12654729,2	K562	blood:
3	chr16:12633130..12635327-chr16:12640812..12643626,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHISA9-4	chr16:12639339-12639458	ENSG00000260601.1
2	lnc-SHISA9-4	chr16:12640142-12640541	ENSG00000260601.1
3	lnc-CPPED1-3	chr16:12650210-12650396	ENSG00000259876.1

No data

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

Extended variants
information (count: 2836 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2836 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8044673	chr16:12632918-12632919	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542687834	chr16:12632923-12632924	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs559686313	chr16:12632926-12632927	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs528417339	chr16:12632945-12632946	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs188027853	chr16:12632947-12632948	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs139467500	chr16:12632948-12632949	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs533222594	chr16:12632955-12632956	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs192591071	chr16:12632978-12632979	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs553307398	chr16:12632981-12632982	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs182371823	chr16:12632989-12632990	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs535453907	chr16:12632994-12632995	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs548993302	chr16:12632998-12632999	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs149889649	chr16:12632999-12633000	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs558042504	chr16:12633001-12633002	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs578127099	chr16:12633004-12633005	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs539189874	chr16:12633013-12633014	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs577396413	chr16:12633015-12633016	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs148646131	chr16:12633025-12633026	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs557085420	chr16:12633027-12633028	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs80044770	chr16:12633041-12633042	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs542624924	chr16:12633042-12633043	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs374836505	chr16:12633044-12633045	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs142915614	chr16:12633060-12633061	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs545289165	chr16:12633063-12633064	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs535129756	chr16:12633069-12633070	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs151094121	chr16:12633070-12633071	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs563419837	chr16:12633075-12633076	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs112160258	chr16:12633079-12633080	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566086907	chr16:12633083-12633084	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs111529437	chr16:12633090-12633091	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs552061441	chr16:12633093-12633094	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs571889334	chr16:12633110-12633111	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs537641305	chr16:12633113-12633114	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs549515748	chr16:12633115-12633116	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs117825374	chr16:12633127-12633128	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs567356944	chr16:12633129-12633130	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs536372629	chr16:12633131-12633132	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs552954675	chr16:12633136-12633137	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs187813487	chr16:12633141-12633142	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs71386711	chr16:12633149-12633150	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs544717276	chr16:12633165-12633166	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs558809841	chr16:12633197-12633198	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs575476721	chr16:12633198-12633199	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs543986993	chr16:12633220-12633221	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs560764681	chr16:12633234-12633235	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs529319809	chr16:12633236-12633237	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs146890540	chr16:12633237-12633238	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs559447983	chr16:12633238-12633239	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs528478807	chr16:12633244-12633245	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs551533371	chr16:12633256-12633257	Enhancers Weak transcription Flanking Active TSS	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:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12613000-12670800	Weak transcription	Pancreas	Pancrea
2	chr16:12625400-12633400	Enhancers	Primary T cells fromperipheralblood	blood
3	chr16:12625800-12643400	Weak transcription	Gastric	stomach
4	chr16:12626600-12634600	Weak transcription	Primary B cells from cord blood	blood
5	chr16:12626800-12636000	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr16:12627000-12642200	Weak transcription	Right Ventricle	heart
7	chr16:12627400-12635800	Weak transcription	Fetal Brain Male	brain
8	chr16:12628200-12633400	Enhancers	Primary B cells from peripheral blood	blood
9	chr16:12630200-12633000	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr16:12630200-12633000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr16:12630400-12637000	Weak transcription	Primary T cells from cord blood	blood
12	chr16:12630400-12638800	Weak transcription	Fetal Thymus	thymus
13	chr16:12630600-12637200	Weak transcription	Spleen	Spleen
14	chr16:12631000-12633200	Enhancers	Colon Smooth Muscle	Colon
15	chr16:12631400-12633600	Enhancers	Brain Anterior Caudate	brain
16	chr16:12631600-12633600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr16:12631800-12633200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr16:12632000-12633000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr16:12632000-12633000	Enhancers	Brain Cingulate Gyrus	brain
20	chr16:12632000-12633000	Enhancers	Brain Hippocampus Middle	brain
21	chr16:12632000-12633200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr16:12632000-12633400	Enhancers	Stomach Smooth Muscle	stomach
23	chr16:12632000-12633600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr16:12632000-12633800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr16:12632000-12633800	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr16:12632000-12634000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr16:12632000-12634200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr16:12632000-12635400	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr16:12632200-12633000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr16:12632200-12633000	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr16:12632200-12633200	Enhancers	HepG2	liver
32	chr16:12632200-12633400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr16:12632200-12633600	Enhancers	Brain Substantia Nigra	brain
34	chr16:12632200-12633600	Enhancers	Esophagus	oesophagus
35	chr16:12632200-12633800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr16:12632200-12633800	Enhancers	HSMMtube	muscle
37	chr16:12632200-12633800	Enhancers	NH-A	brain
38	chr16:12632200-12634000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr16:12632200-12634200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr16:12632200-12634200	Enhancers	NHDF-Ad	bronchial
41	chr16:12632200-12634400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr16:12632200-12634600	Enhancers	HSMM	muscle
43	chr16:12632200-12635000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr16:12632400-12633000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr16:12632400-12633000	Enhancers	Adipose Nuclei	Adipose
46	chr16:12632400-12633000	Enhancers	Brain Angular Gyrus	brain
47	chr16:12632400-12633000	Enhancers	Colonic Mucosa	Colon
48	chr16:12632400-12633200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr16:12632400-12633200	Enhancers	Duodenum Mucosa	Duodenum
50	chr16:12632400-12633200	Enhancers	Duodenum Smooth Muscle	Duodenum

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