Variant report

Variant	esv3351528
Chromosome Location	chr16:46853500-46877470
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:659)
CpG islands
(count:797)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:659 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:46863511-46863984	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:46874238-46874279	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:46865528-46865712	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:46873889-46873891	HepG2	liver:	n/a	n/a
5	ATF2	chr16:46863327-46864110	GM12878	blood:	n/a	n/a
6	ATF2	chr16:46855981-46856766	GM12878	blood:	n/a	n/a
7	ATF2	chr16:46856044-46856624	GM12878	blood:	n/a	n/a
8	ATF3	chr16:46864720-46865028	HepG2	liver:	n/a	n/a
9	BACH1	chr16:46865151-46865673	K562	blood:	n/a	n/a
10	BACH1	chr16:46864874-46865821	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr16:46864381-46864491	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr16:46856078-46856518	GM12878	blood:	n/a	n/a
13	BATF	chr16:46863372-46864016	GM12878	blood:	n/a	n/a
14	BATF	chr16:46856088-46856521	GM12878	blood:	n/a	n/a
15	BCL11A	chr16:46856181-46856530	GM12878	blood:	n/a	chr16:46856476-46856485
16	BCL11A	chr16:46863358-46863690	GM12878	blood:	n/a	chr16:46863681-46863688
17	BCL3	chr16:46856188-46856585	GM12878	blood:	n/a	chr16:46856476-46856485
18	BCLAF1	chr16:46855988-46856728	GM12878	blood:	n/a	chr16:46856476-46856485
19	BCLAF1	chr16:46862212-46862685	GM12878	blood:	n/a	chr16:46862421-46862430
20	BCLAF1	chr16:46864053-46865444	GM12878	blood:	n/a	chr16:46864829-46864838 chr16:46864637-46864650 chr16:46865241-46865254 chr16:46865227-46865236 chr16:46864532-46864541
21	BCLAF1	chr16:46855938-46856575	GM12878	blood:	n/a	chr16:46856476-46856485
22	BHLHE40	chr16:46864639-46864737	K562	blood:	n/a	n/a
23	BHLHE40	chr16:46865135-46865471	HepG2	liver:	n/a	n/a
24	BHLHE40	chr16:46864360-46864598	GM12878	blood:	n/a	chr16:46864569-46864585
25	BHLHE40	chr16:46864962-46865545	K562	blood:	n/a	n/a
26	BHLHE40	chr16:46864947-46865532	GM12878	blood:	n/a	n/a
27	BHLHE40	chr16:46873747-46873775	HepG2	liver:	n/a	n/a
28	BHLHE40	chr16:46864224-46864234	K562	blood:	n/a	n/a
29	BRCA1	chr16:46873983-46874183	HepG2	liver:	n/a	n/a
30	BRCA1	chr16:46865229-46865241	HepG2	liver:	n/a	n/a
31	BRCA1	chr16:46865027-46865502	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr16:46856315-46856327	Hela-S3	cervix:	n/a	n/a
33	CCNT2	chr16:46864300-46865550	K562	blood:	n/a	chr16:46865221-46865230
34	CEBPB	chr16:46863479-46863856	IMR90	lung:	n/a	chr16:46863663-46863676 chr16:46863665-46863676 chr16:46863663-46863674
35	CEBPB	chr16:46866693-46867061	K562	blood:	n/a	chr16:46866866-46866877
36	CEBPB	chr16:46866684-46867081	HepG2	liver:	n/a	chr16:46866866-46866877
37	CEBPB	chr16:46866721-46866963	A549	lung:	n/a	chr16:46866866-46866877
38	CEBPB	chr16:46860619-46860965	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr16:46864917-46865202	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr16:46870941-46871021	H1-hESC	embryonic stem cell:	n/a	chr16:46870988-46870999
41	CEBPB	chr16:46866806-46866919	H1-hESC	embryonic stem cell:	n/a	chr16:46866866-46866877
42	CEBPB	chr16:46870849-46871151	Hela-S3	cervix:	n/a	chr16:46870988-46870999
43	CEBPB	chr16:46866675-46867047	K562	blood:	n/a	chr16:46866866-46866877
44	CEBPB	chr16:46866682-46867024	HepG2	liver:	n/a	chr16:46866866-46866877
45	CEBPB	chr16:46870863-46871061	HepG2	liver:	n/a	chr16:46870988-46870999
46	CEBPB	chr16:46866685-46867144	HepG2	liver:	n/a	chr16:46866866-46866877
47	CEBPB	chr16:46870574-46871173	HepG2	liver:	n/a	chr16:46870988-46870999
48	CEBPB	chr16:46865077-46865087	IMR90	lung:	n/a	n/a
49	CEBPB	chr16:46870822-46871136	A549	lung:	n/a	chr16:46870988-46870999
50	CEBPB	chr16:46866761-46866984	IMR90	lung:	n/a	chr16:46866866-46866877

(count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46864715-46864765	BJ	skin:	n/a
2	chr16:46865118-46865168	A549	lung:	n/a
3	chr16:46865077-46865127	HL-60	blood:	n/a
4	chr16:46865077-46865127	HIPEpiC	eye:	n/a
5	chr16:46864715-46864765	BJ	skin:	n/a
6	chr16:46865118-46865168	A549	lung:	n/a
7	chr16:46865077-46865127	HL-60	blood:	n/a
8	chr16:46865077-46865127	HIPEpiC	eye:	n/a
9	chr16:46865077-46865127	HRPEpiC	eye:	n/a
10	chr16:46865555-46865605	AG09319	gingival:	n/a
11	chr16:46865867-46865917	PFSK-1	brain:	n/a
12	chr16:46864733-46864783	ProgFib	skin:	n/a
13	chr16:46864715-46864765	ProgFib	skin:	n/a
14	chr16:46854830-46854880	AG10803	skin:	n/a
15	chr16:46854830-46854880	AG04449	skin:	fetal
16	chr16:46865118-46865168	Caco-2	colon:	n/a
17	chr16:46865555-46865605	HPAEpiC	pulmonary alveolar:	n/a
18	chr16:46865048-46865098	ECC-1	luminal epithelium:	n/a
19	chr16:46865118-46865168	K562	blood:	n/a
20	chr16:46864733-46864783	GM12878	blood:	n/a
21	chr16:46876498-46876548	SAEC	small airway:	n/a
22	chr16:46865048-46865098	GM19239	blood:	n/a
23	chr16:46876498-46876548	SK-N-SH_RA	brain:	n/a
24	chr16:46865080-46865130	SK-N-SH	brain:	n/a
25	chr16:46854830-46854880	GM12892	blood:	n/a
26	chr16:46864733-46864783	HMEC	breast:	n/a
27	chr16:46865519-46865569	Jurkat	blood:	n/a
28	chr16:46865499-46865549	HRCEpiC	kidney:	n/a
29	chr16:46865867-46865917	SK-N-SH_RA	brain:	n/a
30	chr16:46864733-46864783	AG10803	skin:	n/a
31	chr16:46865118-46865168	NT2-D1	testis:	n/a
32	chr16:46865867-46865917	AoSMC	blood vessel:	n/a
33	chr16:46864715-46864765	HRE	kidney:	n/a
34	chr16:46865048-46865098	GM12891	blood:	n/a
35	chr16:46865499-46865549	BE2_C	brain:	n/a
36	chr16:46864715-46864765	HIPEpiC	eye:	n/a
37	chr16:46865499-46865549	HRE	kidney:	n/a
38	chr16:46865080-46865130	BJ	skin:	n/a
39	chr16:46865118-46865168	HEK293	kidney:	embryo
40	chr16:46876498-46876548	AG09309	skin:	n/a
41	chr16:46865048-46865098	HNPCEpiC	eye:	n/a
42	chr16:46865048-46865098	HMEC	breast:	n/a
43	chr16:46865118-46865168	GM19239	blood:	n/a
44	chr16:46864733-46864783	AG09309	skin:	n/a
45	chr16:46865499-46865549	SK-N-MC	brain:	n/a
46	chr16:46864733-46864783	HEK293	kidney:	embryo
47	chr16:46873954-46874004	HAEpiC	amniotic membrane:	n/a
48	chr16:46865519-46865569	SK-N-SH_RA	brain:	n/a
49	chr16:46876498-46876548	HIPEpiC	eye:	n/a
50	chr16:46854830-46854880	HPAEpiC	pulmonary alveolar:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:46855816..46858578-chr16:46865585..46867919,2	MCF-7	breast:
2	chr1:113161757..113162713-chr16:46864244..46865084,2	Hela-S3	cervix:
3	chr16:46862200..46863851-chr16:46863903..46865483,2	MCF-7	breast:
4	chr16:46855816..46858578-chr16:46865585..46867919,2	MCF-7	breast:
5	chr16:46723042..46725138-chr16:46863743..46865908,3	MCF-7	breast:
6	chr16:46856407..46858707-chr16:46862664..46865192,2	K562	blood:
7	chr16:46852902..46855463-chr16:46861590..46865288,6	K562	blood:
8	chr16:46864940..46866562-chr16:47005297..47007739,2	K562	blood:
9	chr16:46822323..46826613-chr16:46862653..46866542,4	K562	blood:
10	chr16:46717600..46719603-chr16:46859611..46862308,2	K562	blood:
11	chr16:46864725..46865438-chr20:61492684..61493496,2	Hela-S3	cervix:
12	chr16:46781286..46782885-chr16:46859796..46861843,2	K562	blood:
13	chr16:46859122..46862415-chr16:46862444..46865069,3	MCF-7	breast:
14	chr16:46721417..46725620-chr16:46861860..46865482,8	K562	blood:
15	chr16:46721087..46725989-chr16:46862740..46865236,7	K562	blood:
16	chr16:46854177..46856451-chr16:46859236..46861575,2	K562	blood:
17	chr16:46653114..46655726-chr16:46861516..46864110,2	K562	blood:
18	chr16:46822897..46825818-chr16:46857518..46859353,2	K562	blood:
19	chr16:46852133..46853769-chr16:46855489..46857597,2	K562	blood:
20	chr1:22109270..22110054-chr16:46864572..46865525,2	Hela-S3	cervix:
21	chr16:46852133..46853769-chr16:46855489..46857597,2	K562	blood:
22	chr16:46854177..46856451-chr16:46859236..46861575,2	K562	blood:
23	chr16:46857437..46861981-chr16:46862572..46865905,5	MCF-7	breast:

No data

Variant related genes	Relation type
C16orf87	TF binding region
C16orf87	CpG island
ENSG00000116489	chromatin interactions
ENSG00000155330	chromatin interactions
ENSG00000090686	chromatin interactions
ENSG00000069345	chromatin interactions
ENSG00000171241	chromatin interactions
ENSG00000007341	chromatin interactions
ENSG00000069329	chromatin interactions
ENSG00000140795	chromatin interactions
ENSG00000091651	chromatin interactions
ENSG00000101190	chromatin interactions
ENSG00000260782	chromatin interactions

Extended variants
information (count: 721 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:721 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537731975	chr16:46853511-46853512	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs117185987	chr16:46853516-46853517	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs375662510	chr16:46853629-46853630	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs4605188	chr16:46853643-46853644	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536507531	chr16:46853654-46853655	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535815482	chr16:46853666-46853667	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554562582	chr16:46853747-46853748	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs67205347	chr16:46853760-46853761	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs535327253	chr16:46853776-46853777	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553287215	chr16:46853796-46853797	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs146083231	chr16:46853825-46853826	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs578234740	chr16:46853832-46853833	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs545503111	chr16:46853854-46853855	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs569662249	chr16:46853877-46853878	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs534670230	chr16:46853945-46853946	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs553349763	chr16:46853956-46853957	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs568598327	chr16:46854014-46854015	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs575824015	chr16:46854108-46854109	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs543002951	chr16:46854121-46854122	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561338673	chr16:46854134-46854135	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs187772306	chr16:46854166-46854167	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572130974	chr16:46854222-46854223	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs540563257	chr16:46854257-46854258	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189788313	chr16:46854262-46854263	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs183104038	chr16:46854320-46854321	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532205577	chr16:46854539-46854540	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs113170835	chr16:46854569-46854570	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140092328	chr16:46854571-46854572	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs529747966	chr16:46854575-46854576	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547825380	chr16:46854587-46854588	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs187779492	chr16:46854606-46854607	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192701271	chr16:46854660-46854661	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576754069	chr16:46854733-46854734	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553663631	chr16:46854748-46854749	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183635199	chr16:46854756-46854757	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559126458	chr16:46854830-46854831	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539201213	chr16:46854831-46854832	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557597616	chr16:46854834-46854835	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188522278	chr16:46854937-46854938	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs535952125	chr16:46854950-46854951	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs577243412	chr16:46855034-46855035	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs149766993	chr16:46855035-46855036	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536801670	chr16:46855073-46855074	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554659181	chr16:46855074-46855075	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573225889	chr16:46855105-46855106	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540137322	chr16:46855149-46855150	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565162171	chr16:46855154-46855155	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs576740439	chr16:46855175-46855176	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115370670	chr16:46855290-46855291	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562345042	chr16:46855523-46855524	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	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
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46824600-46856000	Weak transcription	Ovary	ovary
2	chr16:46824600-46863800	Weak transcription	Aorta	Aorta
3	chr16:46825000-46855200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr16:46829000-46855000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr16:46829000-46863400	Weak transcription	Fetal Stomach	stomach
6	chr16:46829600-46857600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr16:46829600-46860000	Weak transcription	Fetal Brain Male	brain
8	chr16:46831600-46854600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr16:46831600-46863000	Weak transcription	Fetal Muscle Leg	muscle
10	chr16:46831600-46863800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr16:46832800-46856000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr16:46833600-46863000	Weak transcription	Fetal Thymus	thymus
13	chr16:46833600-46864200	Weak transcription	Pancreas	Pancrea
14	chr16:46834200-46863800	Weak transcription	Placenta	Placenta
15	chr16:46834600-46863800	Weak transcription	Fetal Muscle Trunk	muscle
16	chr16:46834800-46854600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr16:46834800-46857600	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr16:46835000-46855200	Weak transcription	Psoas Muscle	Psoas
19	chr16:46835000-46862800	Weak transcription	HSMMtube	muscle
20	chr16:46836800-46863000	Weak transcription	Colon Smooth Muscle	Colon
21	chr16:46837000-46854800	Weak transcription	Fetal Intestine Large	intestine
22	chr16:46837000-46857600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr16:46837000-46863000	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr16:46839600-46855800	Weak transcription	Small Intestine	intestine
25	chr16:46840000-46856000	Weak transcription	HSMM	muscle
26	chr16:46840000-46857200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr16:46840200-46863800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr16:46841600-46863000	Weak transcription	Thymus	Thymus
29	chr16:46842000-46857200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr16:46842400-46857600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr16:46844000-46854400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr16:46844000-46860600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr16:46844200-46856200	Weak transcription	NH-A	brain
34	chr16:46844200-46860200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr16:46844200-46862000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr16:46844200-46863200	Weak transcription	Adipose Nuclei	Adipose
37	chr16:46844400-46854600	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr16:46844400-46856000	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr16:46844400-46856200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr16:46844400-46860200	Weak transcription	Fetal Lung	lung
41	chr16:46844400-46860600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr16:46844600-46860200	Weak transcription	HUVEC	blood vessel
43	chr16:46845000-46860000	Weak transcription	HepG2	liver
44	chr16:46845200-46863000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr16:46845200-46863400	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr16:46847200-46854800	Weak transcription	Primary B cells from peripheral blood	blood
47	chr16:46847400-46855000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr16:46848400-46864200	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr16:46848600-46862400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr16:46849200-46855600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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