Variant report

Variant	esv1797567
Chromosome Location	chr16:74364773-74464693
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	ARID3A	chr16:74402200-74402343	K562	blood:	n/a	n/a
2	ATF1	chr16:74402006-74402375	K562	blood:	n/a	chr16:74402193-74402207
3	ATF2	chr16:74464112-74464462	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
5	ATF3	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
6	ATF3	chr16:74401853-74402428	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
7	ATF3	chr16:74401940-74402325	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
8	ATF3	chr16:74401896-74402310	K562	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
9	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
10	BACH1	chr16:74402015-74402440	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr16:74398509-74398539	K562	blood:	n/a	n/a
12	BATF	chr16:74463982-74464267	GM12878	blood:	n/a	n/a
13	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
14	BHLHE40	chr16:74463888-74464257	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
15	BHLHE40	chr16:74401339-74402424	K562	blood:	n/a	n/a
16	BHLHE40	chr16:74463926-74464447	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
17	BHLHE40	chr16:74463908-74464447	K562	blood:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
18	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
19	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
20	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
21	BHLHE40	chr16:74464015-74464235	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
22	BHLHE40	chr16:74463983-74464410	GM12878	blood:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
23	BHLHE40	chr16:74445450-74445698	HepG2	liver:	n/a	n/a
24	BHLHE40	chr16:74464001-74464283	A549	lung:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
25	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
26	BRCA1	chr16:74402144-74402372	HepG2	liver:	n/a	chr16:74402243-74402252
27	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
28	BRCA1	chr16:74398022-74398270	HepG2	liver:	n/a	n/a
29	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
30	BRCA1	chr16:74464034-74464229	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252
32	CBX3	chr16:74401099-74402880	K562	blood:	n/a	n/a
33	CCNT2	chr16:74401990-74402360	K562	blood:	n/a	chr16:74402213-74402222 chr16:74402077-74402086
34	CEBPB	chr16:74408261-74408362	HepG2	liver:	n/a	chr16:74408302-74408313
35	CEBPB	chr16:74367000-74367116	K562	blood:	n/a	n/a
36	CEBPB	chr16:74441969-74442184	K562	blood:	n/a	n/a
37	CEBPB	chr16:74404669-74404976	K562	blood:	n/a	n/a
38	CEBPB	chr16:74408185-74408404	Hela-S3	cervix:	n/a	chr16:74408302-74408313
39	CEBPB	chr16:74404767-74404870	HepG2	liver:	n/a	n/a
40	CEBPB	chr16:74408191-74408395	K562	blood:	n/a	chr16:74408302-74408313
41	CEBPB	chr16:74408152-74408392	HepG2	liver:	n/a	chr16:74408302-74408313
42	CEBPB	chr16:74366899-74367207	HepG2	liver:	n/a	n/a
43	CEBPD	chr16:74401789-74402094	HepG2	liver:	n/a	n/a
44	CEBPD	chr16:74401797-74402467	K562	blood:	n/a	n/a
45	CEBPD	chr16:74462586-74462902	K562	blood:	n/a	n/a
46	CHD1	chr16:74401791-74401985	GM12878	blood:	n/a	n/a
47	CHD2	chr16:74464067-74464110	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr16:74402129-74402399	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
49	CHD2	chr16:74402024-74402427	K562	blood:	n/a	chr16:74402243-74402252 chr16:74402078-74402088
50	CHD2	chr16:74401964-74402403	Hela-S3	cervix:	n/a	chr16:74402243-74402252 chr16:74402078-74402088

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74441639-74441689	HL-60	blood:	n/a
2	chr16:74455448-74455498	AG04450	lung:	fetal
3	chr16:74441639-74441689	HL-60	blood:	n/a
4	chr16:74455448-74455498	AG04450	lung:	fetal
5	chr16:74400946-74400996	NT2-D1	testis:	n/a
6	chr16:74401794-74401844	PrEC	prostate:	n/a
7	chr16:74441639-74441689	AG09309	skin:	n/a
8	chr16:74402329-74402379	HIPEpiC	eye:	n/a
9	chr16:74401986-74402036	K562	blood:	n/a
10	chr16:74401547-74401597	IMR90	lung:	fetal
11	chr16:74455448-74455498	HIPEpiC	eye:	n/a
12	chr16:74456200-74456250	HEK293	kidney:	embryo
13	chr16:74401986-74402036	LNCaP	prostate:	n/a
14	chr16:74455448-74455498	AG04449	skin:	fetal
15	chr16:74441639-74441689	Caco-2	colon:	n/a
16	chr16:74401547-74401597	BE2_C	brain:	n/a
17	chr16:74455562-74455612	IMR90	lung:	fetal
18	chr16:74402336-74402386	BJ	skin:	n/a
19	chr16:74403516-74403566	T-47D	breast:	n/a
20	chr16:74403516-74403566	LNCaP	prostate:	n/a
21	chr16:74455562-74455612	ProgFib	skin:	n/a
22	chr16:74455448-74455498	LNCaP	prostate:	n/a
23	chr16:74401547-74401597	GM12891	blood:	n/a
24	chr16:74446218-74446268	GM12892	blood:	n/a
25	chr16:74455562-74455612	LNCaP	prostate:	n/a
26	chr16:74446218-74446268	HRCEpiC	kidney:	n/a
27	chr16:74406059-74406109	GM06990	blood:	n/a
28	chr16:74455360-74455410	SAEC	small airway:	n/a
29	chr16:74402329-74402379	MCF10A-Er-Src	breast:	n/a
30	chr16:74446218-74446268	HRPEpiC	eye:	n/a
31	chr16:74401547-74401597	AG09309	skin:	n/a
32	chr16:74402329-74402379	MCF-7	breast:	n/a
33	chr16:74401986-74402036	HUVEC	blood vessel:	n/a
34	chr16:74446218-74446268	SKMC	muscle:	n/a
35	chr16:74446218-74446268	Hepatocyte	liver:	n/a
36	chr16:74455448-74455498	IMR90	lung:	fetal
37	chr16:74456200-74456250	PFSK-1	brain:	n/a
38	chr16:74400946-74400996	Hela-S3	cervix:	n/a
39	chr16:74398168-74398218	GM06990	blood:	n/a
40	chr16:74402329-74402379	GM06990	blood:	n/a
41	chr16:74406059-74406109	HCM	heart:	n/a
42	chr16:74446218-74446268	HNPCEpiC	eye:	n/a
43	chr16:74401986-74402036	SAEC	small airway:	n/a
44	chr16:74456200-74456250	HRE	kidney:	n/a
45	chr16:74455562-74455612	HCT-116	colon:	n/a
46	chr16:74402329-74402379	AG09319	gingival:	n/a
47	chr16:74401986-74402036	RPTEC	kidney:	n/a
48	chr16:74400946-74400996	NHDF-neo	bronchial:	n/a
49	chr16:74456200-74456250	Hela-S3	cervix:	n/a
50	chr16:74406059-74406109	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr16:74463888..74464834-chr16:74487133..74487740,2	MCF-7	breast:
2	chr16:74394116..74395645-chr3:9438342..9440027,2	MCF-7	breast:
3	chr16:70185001..70186006-chr16:74463672..74464734,4	MCF-7	breast:
4	chr16:74329306..74331523-chr16:74400690..74402975,2	MCF-7	breast:
5	chr16:74396107..74397775-chr16:74400703..74403254,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPIPL2-2	chr16:74456028-74456340	ENSG00000261170.1
2	lnc-CLEC18B-1	chr16:74411388-74411587	XLOC_012009
3	lnc-NPIPL2-2	chr16:74456018-74456340	ENSG00000261170.1
4	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
5	lnc-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1
6	lnc-NPIPL2-3	chr16:74389382-74389428	l_1361_chr16:74389381-74506276_brain
7	lnc-CLEC18B-1	chr16:74411642-74411717	XLOC_012009
8	lnc-CLEC18B-2	chr16:74368790-74369244	ENSG00000259972.1
9	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681

Variant related genes	Relation type
NPIPB15	TF binding region
ENSG00000259972	TF binding region
ENSG00000261079	TF binding region
CLEC18B	TF binding region
ENSG00000261170	TF binding region
ENSG00000214331	TF binding region
NPIPB15	CpG island
ENSG00000259972	CpG island
ENSG00000261079	CpG island
CLEC18B	CpG island
ENSG00000261170	CpG island
ENSG00000214331	CpG island
ENSG00000168137	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000261079	chromatin interactions
ENSG00000214331	chromatin interactions
ENSG00000206573	chromatin interactions

Extended variants
information (count: 4153 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4153 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28653489	chr16:74364809-74364810	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs28549800	chr16:74364811-74364812	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs528845448	chr16:74364834-74364835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548981462	chr16:74364875-74364876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185832373	chr16:74364893-74364894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141647565	chr16:74364913-74364914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150085170	chr16:74364930-74364931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551587093	chr16:74364936-74364937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114510280	chr16:74364943-74364944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557244815	chr16:74364964-74364965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1318113	chr16:74364978-74364979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34810197	chr16:74364983-74364984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573887001	chr16:74364992-74364993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536215394	chr16:74365020-74365021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553351456	chr16:74365028-74365029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2869601	chr16:74365033-74365034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2869121	chr16:74365047-74365048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545518004	chr16:74365066-74365067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565126347	chr16:74365085-74365086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1318112	chr16:74365097-74365098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs16973221	chr16:74365098-74365099	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs544413107	chr16:74365106-74365107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531958443	chr16:74365107-74365108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2860552	chr16:74365113-74365114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181068373	chr16:74365120-74365121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530445285	chr16:74365127-74365128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34435893	chr16:74365140-74365141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142752090	chr16:74365150-74365151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552010455	chr16:74365174-74365175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113322051	chr16:74365181-74365182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34755812	chr16:74365200-74365201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9936663	chr16:74365218-74365219	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs186100497	chr16:74365231-74365232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530681631	chr16:74365239-74365240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9929478	chr16:74365283-74365284	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs11648396	chr16:74365290-74365291	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs2911033	chr16:74365298-74365299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2911032	chr16:74365308-74365309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553076646	chr16:74365316-74365317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142299398	chr16:74365330-74365331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538743470	chr16:74365342-74365343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558588246	chr16:74365348-74365349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370866767	chr16:74365450-74365451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576602065	chr16:74365454-74365455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575350306	chr16:74365464-74365465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34379512	chr16:74365469-74365470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190626946	chr16:74365517-74365518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567745446	chr16:74365577-74365578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183340131	chr16:74365583-74365584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187645260	chr16:74365590-74365591	Weak transcription Strong transcription	n/a	n/a	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	21364760	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	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

Chromatin state (count:1935 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74331800-74366400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:74332800-74401200	Weak transcription	Stomach Mucosa	stomach
3	chr16:74339600-74394000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr16:74340600-74387000	Weak transcription	Hela-S3	cervix
5	chr16:74340800-74400200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr16:74341400-74366600	Weak transcription	A549	lung
7	chr16:74341400-74371600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr16:74341400-74376200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr16:74341400-74400800	Weak transcription	NH-A	brain
10	chr16:74341600-74366400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr16:74341600-74371200	Weak transcription	HUVEC	blood vessel
12	chr16:74355200-74400800	Weak transcription	Fetal Brain Male	brain
13	chr16:74355600-74382200	Weak transcription	GM12878-XiMat	blood
14	chr16:74356600-74371400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr16:74357600-74367600	Strong transcription	Fetal Stomach	stomach
16	chr16:74357800-74367600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr16:74358200-74367200	Strong transcription	Fetal Intestine Small	intestine
18	chr16:74359400-74367200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr16:74360000-74364800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr16:74360000-74378200	Weak transcription	Primary B cells from cord blood	blood
21	chr16:74360000-74401400	Weak transcription	Small Intestine	intestine
22	chr16:74360600-74364800	Weak transcription	Brain Germinal Matrix	brain
23	chr16:74360600-74364800	Weak transcription	NHLF	lung
24	chr16:74360600-74366600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr16:74360600-74371600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr16:74360600-74382600	Weak transcription	HSMMtube	muscle
27	chr16:74360800-74364800	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr16:74360800-74364800	Weak transcription	Right Ventricle	heart
29	chr16:74360800-74366400	Weak transcription	Brain Angular Gyrus	brain
30	chr16:74360800-74383000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr16:74361000-74364800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr16:74361000-74366000	Weak transcription	Fetal Lung	lung
33	chr16:74361000-74366400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr16:74361000-74366600	Weak transcription	Colon Smooth Muscle	Colon
35	chr16:74361000-74382000	Weak transcription	Fetal Kidney	kidney
36	chr16:74361000-74385000	Weak transcription	K562	blood
37	chr16:74361400-74384200	Weak transcription	Primary hematopoietic stem cells	blood
38	chr16:74362000-74364800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr16:74362000-74366600	Weak transcription	Aorta	Aorta
40	chr16:74362000-74400400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr16:74362200-74364800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr16:74362200-74366000	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr16:74362200-74366200	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr16:74362200-74387400	Weak transcription	NHDF-Ad	bronchial
45	chr16:74362200-74392400	Weak transcription	HSMM	muscle
46	chr16:74362200-74394000	Weak transcription	HMEC	breast
47	chr16:74362200-74398600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr16:74362800-74398000	Weak transcription	Psoas Muscle	Psoas
49	chr16:74363400-74367200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr16:74363800-74367200	Strong transcription	Stomach Smooth Muscle	stomach

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