Variant report

Variant	esv2750743
Chromosome Location	chr16:75558545-75580137
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:89)
CpG islands
(count:917)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:89 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:75561718-75562303	HepG2	liver:	n/a	n/a
2	BHLHE40	chr16:75559972-75560220	K562	blood:	n/a	n/a
3	BHLHE40	chr16:75563977-75564136	K562	blood:	n/a	n/a
4	CEBPB	chr16:75565147-75565217	K562	blood:	n/a	n/a
5	CTCF	chr16:75579545-75579583	LNCaP	prostate:	n/a	n/a
6	CTCF	chr16:75579352-75579407	GM20000	blood:	n/a	n/a
7	CTCF	chr16:75559060-75559210	GM12869	blood:	n/a	n/a
8	CTCF	chr16:75560108-75560140	Pancreas_OC	pancreas:	n/a	n/a
9	CTCF	chr16:75563724-75563771	Lung_OC	lung:	n/a	n/a
10	CTCF	chr16:75562800-75562950	GM12866	blood:	n/a	n/a
11	CTCF	chr16:75569840-75569990	HBMEC	blood vessel:	n/a	chr16:75569964-75569977
12	CTCF	chr16:75560048-75560124	GM19239	blood:	n/a	n/a
13	CUX1	chr16:75578446-75578511	K562	blood:	n/a	n/a
14	E2F6	chr16:75563962-75564175	K562	blood:	n/a	n/a
15	FOSL2	chr16:75561614-75562031	HepG2	liver:	n/a	chr16:75561806-75561817
16	FOSL2	chr16:75572989-75573380	HepG2	liver:	n/a	n/a
17	FOSL2	chr16:75561638-75562060	HepG2	liver:	n/a	chr16:75561806-75561817
18	FOXA1	chr16:75561674-75562137	HepG2	liver:	n/a	n/a
19	FOXA1	chr16:75561643-75562160	HepG2	liver:	n/a	n/a
20	FOXA1	chr16:75561660-75562153	HepG2	liver:	n/a	n/a
21	FOXA1	chr16:75561641-75562165	HepG2	liver:	n/a	n/a
22	FOXA2	chr16:75561742-75562084	HepG2	liver:	n/a	n/a
23	GABPA	chr16:75559970-75560194	HepG2	liver:	n/a	n/a
24	HDAC2	chr16:75561738-75562098	HepG2	liver:	n/a	n/a
25	HMGN3	chr16:75563086-75563460	K562	blood:	n/a	n/a
26	HNF4A	chr16:75561739-75562068	HepG2	liver:	n/a	n/a
27	HNF4A	chr16:75561741-75562050	HepG2	liver:	n/a	n/a
28	HNF4G	chr16:75561730-75562102	HepG2	liver:	n/a	chr16:75561920-75561935
29	IRF1	chr16:75574300-75574692	K562	blood:	n/a	chr16:75574525-75574545 chr16:75574532-75574545 chr16:75574530-75574544 chr16:75574531-75574545 chr16:75574532-75574545 chr16:75574531-75574542 chr16:75574533-75574543 chr16:75574531-75574551 chr16:75574527-75574544 chr16:75574533-75574547 chr16:75574532-75574545 chr16:75574529-75574543 chr16:75574532-75574546 chr16:75574532-75574543
30	IRF1	chr16:75574370-75574557	K562	blood:	n/a	chr16:75574525-75574545 chr16:75574532-75574545 chr16:75574530-75574544 chr16:75574531-75574545 chr16:75574532-75574545 chr16:75574531-75574542 chr16:75574533-75574543 chr16:75574531-75574551 chr16:75574527-75574544 chr16:75574533-75574547 chr16:75574532-75574545 chr16:75574529-75574543 chr16:75574532-75574546 chr16:75574532-75574543
31	JUND	chr16:75561735-75561872	HepG2	liver:	n/a	chr16:75561805-75561816
32	JUND	chr16:75561705-75562019	HepG2	liver:	n/a	chr16:75561805-75561816
33	JUND	chr16:75561985-75562005	H1-hESC	embryonic stem cell:	n/a	n/a
34	JUND	chr16:75573154-75573383	HepG2	liver:	n/a	n/a
35	MAX	chr16:75560106-75560134	HepG2	liver:	n/a	n/a
36	MAX	chr16:75564006-75564146	K562	blood:	n/a	n/a
37	MAX	chr16:75563866-75564244	K562	blood:	n/a	n/a
38	MYBL2	chr16:75561676-75562202	HepG2	liver:	n/a	n/a
39	MYC	chr16:75571882-75571911	K562	blood:	n/a	n/a
40	MYC	chr16:75572718-75572737	H1-hESC	embryonic stem cell:	n/a	n/a
41	NFYB	chr16:75562030-75562273	GM12878	blood:	n/a	n/a
42	POLR2A	chr16:75568871-75568878	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr16:75572587-75572841	MCF-7	breast:	n/a	n/a
44	POLR2A	chr16:75579329-75579348	MCF-7	breast:	n/a	n/a
45	POLR2A	chr16:75569716-75569916	K562	blood:	n/a	n/a
46	POLR2A	chr16:75575234-75575307	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr16:75569311-75569507	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr16:75569748-75570077	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr16:75572634-75572683	Gliobla	brain:	n/a	n/a
50	POLR2A	chr16:75579314-75579352	MCF-7	breast:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:75568999-75569049	HEK293	kidney:	embryo
2	chr16:75569459-75569509	HIPEpiC	eye:	n/a
3	chr16:75568999-75569049	HEK293	kidney:	embryo
4	chr16:75569459-75569509	HIPEpiC	eye:	n/a
5	chr16:75569164-75569214	GM19239	blood:	n/a
6	chr16:75569164-75569214	PFSK-1	brain:	n/a
7	chr16:75569459-75569509	LNCaP	prostate:	n/a
8	chr16:75563489-75563539	T-47D	breast:	n/a
9	chr16:75563280-75563330	Caco-2	colon:	n/a
10	chr16:75572883-75572933	Jurkat	blood:	n/a
11	chr16:75563489-75563539	NHBE	bronchial:	n/a
12	chr16:75569164-75569214	BJ	skin:	n/a
13	chr16:75563009-75563059	HIPEpiC	eye:	n/a
14	chr16:75569164-75569214	SK-N-SH	brain:	n/a
15	chr16:75569459-75569509	PFSK-1	brain:	n/a
16	chr16:75568999-75569049	SAEC	small airway:	n/a
17	chr16:75569459-75569509	SK-N-MC	brain:	n/a
18	chr16:75563489-75563539	MCF10A-Er-Src	breast:	n/a
19	chr16:75569164-75569214	HCPEpiC	choroid plexus:	n/a
20	chr16:75572883-75572933	K562	blood:	n/a
21	chr16:75563901-75563951	HL-60	blood:	n/a
22	chr16:75569527-75569577	Jurkat	blood:	n/a
23	chr16:75563114-75563164	HIPEpiC	eye:	n/a
24	chr16:75563280-75563330	HCF	heart:	n/a
25	chr16:75568999-75569049	AoSMC	blood vessel:	n/a
26	chr16:75563901-75563951	HRPEpiC	eye:	n/a
27	chr16:75572883-75572933	SAEC	small airway:	n/a
28	chr16:75563901-75563951	NH-A	brain:	n/a
29	chr16:75564221-75564271	H1-hESC	embryonic stem cell:	embryo
30	chr16:75569164-75569214	AoSMC	blood vessel:	n/a
31	chr16:75559912-75559962	NHDF-neo	bronchial:	n/a
32	chr16:75569852-75569902	GM19239	blood:	n/a
33	chr16:75563489-75563539	HL-60	blood:	n/a
34	chr16:75575906-75575956	AG04449	skin:	fetal
35	chr16:75569459-75569509	BJ	skin:	n/a
36	chr16:75559912-75559962	GM12891	blood:	n/a
37	chr16:75566465-75566515	GM12878	blood:	n/a
38	chr16:75563901-75563951	AoSMC	blood vessel:	n/a
39	chr16:75569527-75569577	AG09309	skin:	n/a
40	chr16:75568999-75569049	GM19239	blood:	n/a
41	chr16:75564221-75564271	HepG2	liver:	n/a
42	chr16:75569852-75569902	AoSMC	blood vessel:	n/a
43	chr16:75563280-75563330	GM06990	blood:	n/a
44	chr16:75569527-75569577	HAEpiC	amniotic membrane:	n/a
45	chr16:75569852-75569902	NH-A	brain:	n/a
46	chr16:75566465-75566515	BJ	skin:	n/a
47	chr16:75568999-75569049	NHDF-neo	bronchial:	n/a
48	chr16:75569459-75569509	SKMC	muscle:	n/a
49	chr16:75563280-75563330	LNCaP	prostate:	n/a
50	chr16:75569459-75569509	Caco-2	colon:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:75574159..75575888-chr16:75581471..75583351,2	K562	blood:
2	chr16:75539405..75540962-chr16:75572342..75574110,2	K562	blood:
3	chr16:75576612..75578705-chr16:75660423..75663143,2	K562	blood:
4	chr16:75564501..75567219-chr16:75571368..75573194,2	K562	blood:
5	chr16:75574449..75576989-chr16:75588011..75589806,2	K562	blood:
6	chr16:75538464..75540762-chr16:75575477..75578098,2	MCF-7	breast:
7	chr16:75550465..75552637-chr16:75558863..75560839,2	K562	blood:
8	chr16:75572249..75573874-chr16:75680228..75682477,2	MCF-7	breast:
9	chr16:75533525..75534182-chr16:75573663..75574408,2	MCF-7	breast:
10	chr16:75564501..75567085-chr16:75571192..75573194,2	K562	blood:
11	chr16:75570762..75572723-chr16:75573865..75576124,2	K562	blood:
12	chr16:75563203..75565512-chr16:75568208..75570282,2	K562	blood:
13	chr16:75574262..75576234-chr16:75588612..75590836,2	MCF-7	breast:
14	chr16:75560467..75563051-chr16:75574303..75577807,3	K562	blood:
15	chr16:75566186..75568910-chr16:75569034..75571524,2	MCF-7	breast:
16	chr16:75553671..75555315-chr16:75557566..75560051,2	K562	blood:
17	chr16:75497125..75499382-chr16:75564750..75566395,2	MCF-7	breast:
18	chr16:75554663..75556998-chr16:75557661..75561177,3	MCF-7	breast:
19	chr16:75549910..75552098-chr16:75575318..75577076,2	MCF-7	breast:
20	chr16:75550093..75552662-chr16:75555464..75560053,5	MCF-7	breast:
21	chr16:75564094..75567077-chr16:75588072..75589709,2	K562	blood:
22	chr16:75568229..75570112-chr16:75587872..75589519,2	K562	blood:

No data

Variant related genes	Relation type
CHST5	TF binding region
TMEM231	TF binding region
ENSG00000260092	TF binding region
CHST5	CpG island
TMEM231	CpG island
ENSG00000260092	CpG island
ENSG00000261717	chromatin interactions
ENSG00000166822	chromatin interactions
ENSG00000205084	chromatin interactions
ENSG00000135702	chromatin interactions
ENSG00000166848	chromatin interactions
ENSG00000065427	chromatin interactions
ENSG00000262583	chromatin interactions

Extended variants
information (count: 1121 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1121 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576175040	chr16:75558566-75558567	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs541923389	chr16:75558570-75558571	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555534374	chr16:75558673-75558674	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572536328	chr16:75558677-75558678	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs149190976	chr16:75558690-75558691	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183259383	chr16:75558709-75558710	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs371844775	chr16:75558716-75558717	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs79748594	chr16:75558769-75558770	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543383263	chr16:75558809-75558810	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2738794	chr16:75558810-75558811	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529282220	chr16:75558812-75558813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs143363632	chr16:75558830-75558831	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs549054775	chr16:75558843-75558844	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs117071846	chr16:75558930-75558931	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs137997103	chr16:75558958-75558959	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs548672027	chr16:75558978-75558979	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187989348	chr16:75558983-75558984	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547426088	chr16:75558984-75558985	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569805963	chr16:75559008-75559009	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561042019	chr16:75559062-75559063	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs143493013	chr16:75559082-75559083	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs191998195	chr16:75559145-75559146	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs550013793	chr16:75559229-75559230	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556528475	chr16:75559246-75559247	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs147170458	chr16:75559250-75559251	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs73612847	chr16:75559273-75559274	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs75586499	chr16:75559308-75559309	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs138610571	chr16:75559344-75559345	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534865395	chr16:75559445-75559446	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558346225	chr16:75559551-75559552	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs578130023	chr16:75559578-75559579	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs368792341	chr16:75559588-75559589	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs141151596	chr16:75559602-75559603	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2641807	chr16:75559619-75559620	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs184601668	chr16:75559689-75559690	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542613016	chr16:75559717-75559718	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs150796747	chr16:75559722-75559723	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs187784976	chr16:75559729-75559730	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116970789	chr16:75559745-75559746	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564287540	chr16:75559763-75559764	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs71394223	chr16:75559785-75559786	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533198515	chr16:75559794-75559795	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs550091637	chr16:75559806-75559807	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs112631900	chr16:75559812-75559813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376025871	chr16:75559813-75559814	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs570013026	chr16:75559821-75559822	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs369537073	chr16:75559871-75559872	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139220648	chr16:75559884-75559885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs549009219	chr16:75559904-75559905	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565605324	chr16:75559946-75559947	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75551200-75566400	Weak transcription	Brain Substantia Nigra	brain
2	chr16:75551200-75589200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:75551400-75562800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr16:75551400-75562800	Weak transcription	Small Intestine	intestine
5	chr16:75551400-75572200	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr16:75551400-75584000	Weak transcription	Right Atrium	heart
7	chr16:75551600-75561800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr16:75551600-75562800	Weak transcription	Brain Angular Gyrus	brain
9	chr16:75551600-75563000	Weak transcription	Ovary	ovary
10	chr16:75551600-75568400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr16:75551600-75575800	Weak transcription	Brain Hippocampus Middle	brain
12	chr16:75551800-75558800	Weak transcription	Brain Anterior Caudate	brain
13	chr16:75551800-75558800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr16:75551800-75561600	Weak transcription	Colonic Mucosa	Colon
15	chr16:75551800-75561600	Weak transcription	Fetal Intestine Small	intestine
16	chr16:75551800-75563000	Weak transcription	Brain Germinal Matrix	brain
17	chr16:75551800-75563000	Weak transcription	Fetal Stomach	stomach
18	chr16:75551800-75572400	Weak transcription	Right Ventricle	heart
19	chr16:75551800-75578000	Weak transcription	Fetal Brain Female	brain
20	chr16:75557800-75572400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr16:75558000-75558800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr16:75558000-75560200	Strong transcription	Duodenum Mucosa	Duodenum
23	chr16:75558000-75560600	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr16:75558000-75560600	Strong transcription	Rectal Mucosa Donor 31	rectum
25	chr16:75558200-75560200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr16:75558400-75558600	Enhancers	Stomach Mucosa	stomach
27	chr16:75558600-75561400	Weak transcription	Stomach Mucosa	stomach
28	chr16:75558600-75572000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr16:75558800-75560200	Strong transcription	Brain Anterior Caudate	brain
30	chr16:75558800-75560400	Strong transcription	Brain Inferior Temporal Lobe	brain
31	chr16:75559600-75559800	Enhancers	Fetal Intestine Large	intestine
32	chr16:75559600-75560000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr16:75559800-75561400	Weak transcription	Fetal Intestine Large	intestine
34	chr16:75560000-75560200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr16:75560000-75560200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr16:75560000-75560200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr16:75560000-75560200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr16:75560200-75560600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr16:75560200-75562000	Weak transcription	Duodenum Mucosa	Duodenum
40	chr16:75560200-75563000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr16:75560200-75563000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr16:75560200-75563000	Weak transcription	Brain Anterior Caudate	brain
43	chr16:75560200-75563800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr16:75560200-75566400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr16:75560400-75560600	Enhancers	Fetal Muscle Leg	muscle
46	chr16:75560400-75562600	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr16:75560600-75562000	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr16:75560600-75562000	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr16:75560600-75568600	Weak transcription	Fetal Muscle Leg	muscle
50	chr16:75561400-75562400	Enhancers	Fetal Intestine Large	intestine

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