Variant report

Variant	nsv906932
Chromosome Location	chr16:75898641-76069129
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	BACH1	chr16:75955241-75955473	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr16:75955179-75955438	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr16:76027103-76027303	K562	blood:	n/a	n/a
4	CEBPB	chr16:75986034-75986327	A549	lung:	n/a	chr16:75986219-75986230
5	CEBPB	chr16:76057114-76057273	K562	blood:	n/a	chr16:76057208-76057219 chr16:76057206-76057219 chr16:76057206-76057217
6	CEBPB	chr16:76057128-76057349	HepG2	liver:	n/a	chr16:76057208-76057219 chr16:76057206-76057219 chr16:76057206-76057217
7	CEBPB	chr16:75962224-75962687	IMR90	lung:	n/a	chr16:75962657-75962670 chr16:75962659-75962670 chr16:75962657-75962670 chr16:75962659-75962670
8	CEBPB	chr16:75917317-75917473	HepG2	liver:	n/a	chr16:75917402-75917413
9	CEBPB	chr16:76017149-76017155	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr16:76005267-76005573	A549	lung:	n/a	chr16:76005416-76005427
11	CEBPB	chr16:76005256-76005605	IMR90	lung:	n/a	chr16:76005416-76005427
12	CEBPB	chr16:75964903-75965356	IMR90	lung:	n/a	n/a
13	CEBPB	chr16:75945831-75946128	A549	lung:	n/a	chr16:75945976-75945987
14	CEBPB	chr16:76052058-76052258	HepG2	liver:	n/a	chr16:76052151-76052162 chr16:76052153-76052162
15	CEBPB	chr16:75991954-75992175	IMR90	lung:	n/a	chr16:75992023-75992036
16	CEBPB	chr16:76045003-76045214	HepG2	liver:	n/a	n/a
17	CEBPB	chr16:75999192-75999437	HepG2	liver:	n/a	chr16:75999316-75999329 chr16:75999316-75999329 chr16:75999315-75999332 chr16:75999304-75999317 chr16:75999317-75999328
18	CEBPB	chr16:76019939-76020108	HepG2	liver:	n/a	chr16:76020002-76020013
19	CEBPB	chr16:76010225-76010506	A549	lung:	n/a	chr16:76010399-76010412 chr16:76010400-76010411 chr16:76010399-76010412 chr16:76010355-76010366
20	CEBPB	chr16:76005242-76005604	K562	blood:	n/a	chr16:76005416-76005427
21	CEBPB	chr16:75945836-75946142	HepG2	liver:	n/a	chr16:75945976-75945987
22	CEBPB	chr16:75994433-75994734	HepG2	liver:	n/a	chr16:75994578-75994589
23	CEBPB	chr16:76030246-76030368	HepG2	liver:	n/a	n/a
24	CEBPB	chr16:75986137-75986264	K562	blood:	n/a	chr16:75986219-75986230
25	CEBPB	chr16:76010178-76010546	HepG2	liver:	n/a	chr16:76010399-76010412 chr16:76010400-76010411 chr16:76010399-76010412 chr16:76010355-76010366
26	CEBPB	chr16:75986066-75986378	IMR90	lung:	n/a	chr16:75986219-75986230
27	CEBPB	chr16:76010243-76010487	IMR90	lung:	n/a	chr16:76010399-76010412 chr16:76010400-76010411 chr16:76010399-76010412 chr16:76010355-76010366
28	CEBPB	chr16:76005299-76005553	H1-hESC	embryonic stem cell:	n/a	chr16:76005416-76005427
29	CEBPB	chr16:75994457-75994683	IMR90	lung:	n/a	chr16:75994578-75994589
30	CEBPB	chr16:75986058-75986398	HepG2	liver:	n/a	chr16:75986219-75986230
31	CEBPB	chr16:75945872-75946120	Hela-S3	cervix:	n/a	chr16:75945976-75945987
32	CEBPB	chr16:76005249-76005589	HepG2	liver:	n/a	chr16:76005416-76005427
33	CEBPB	chr16:75945837-75946101	IMR90	lung:	n/a	chr16:75945976-75945987
34	CEBPB	chr16:75944172-75944230	HepG2	liver:	n/a	n/a
35	CEBPB	chr16:75992000-75992124	HepG2	liver:	n/a	chr16:75992023-75992036
36	CEBPB	chr16:75986087-75986315	H1-hESC	embryonic stem cell:	n/a	chr16:75986219-75986230
37	CEBPB	chr16:76057066-76057317	A549	lung:	n/a	chr16:76057208-76057219 chr16:76057206-76057219 chr16:76057206-76057217
38	CHD1	chr16:75961618-75961764	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr16:75958920-75959070	MCF-7	breast:	n/a	n/a
40	CTCF	chr16:75959028-75959153	MCF-7	breast:	n/a	n/a
41	CTCF	chr16:75903240-75903390	MCF-7	breast:	n/a	n/a
42	CTCF	chr16:75942800-75942950	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr16:75904855-75904926	GM20000	blood:	n/a	n/a
44	CTCF	chr16:75959050-75959142	MCF-7	breast:	n/a	n/a
45	CTCF	chr16:76027290-76027321	K562	blood:	n/a	n/a
46	CTCF	chr16:75937920-75938070	HRE	kidney:	n/a	n/a
47	CTCF	chr16:75958614-75958675	ProgFib	skin:	n/a	n/a
48	CTCF	chr16:75959061-75959135	MCF-7	breast:	n/a	n/a
49	CTCF	chr16:75956900-75957050	HEEpiC	esophagus:	n/a	chr16:75956974-75956982
50	CTCF	chr16:75992320-75992470	GM12868	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:75964393-75964443	BE2_C	brain:	n/a
2	chr16:75964393-75964443	HCPEpiC	choroid plexus:	n/a
3	chr16:75964393-75964443	GM12892	blood:	n/a
4	chr16:75964393-75964443	HPAEpiC	pulmonary alveolar:	n/a
5	chr16:75964393-75964443	NHBE	bronchial:	n/a
6	chr16:75964393-75964443	SK-N-MC	brain:	n/a
7	chr16:75964393-75964443	AG10803	skin:	n/a
8	chr16:75964393-75964443	AG04450	lung:	fetal
9	chr16:75964393-75964443	SAEC	small airway:	n/a
10	chr16:75964393-75964443	SK-N-SH_RA	brain:	n/a
11	chr16:75964393-75964443	PFSK-1	brain:	n/a
12	chr16:75964393-75964443	Hepatocyte	liver:	n/a
13	chr16:75964393-75964443	HAEpiC	amniotic membrane:	n/a
14	chr16:75964393-75964443	HCF	heart:	n/a
15	chr16:75964393-75964443	U87	brain:	n/a
16	chr16:75964393-75964443	HRE	kidney:	n/a
17	chr16:75964393-75964443	CMK	blood:	n/a
18	chr16:75964393-75964443	LNCaP	prostate:	n/a
19	chr16:75964393-75964443	MCF-7	breast:	n/a
20	chr16:75964393-75964443	HCM	heart:	n/a
21	chr16:75964393-75964443	K562	blood:	n/a
22	chr16:75964393-75964443	H1-hESC	embryonic stem cell:	embryo
23	chr16:75964393-75964443	HEK293	kidney:	embryo
24	chr16:75964393-75964443	Caco-2	colon:	n/a
25	chr16:75964393-75964443	MCF10A-Er-Src	breast:	n/a
26	chr16:75964393-75964443	PrEC	prostate:	n/a
27	chr16:75964393-75964443	HCT-116	colon:	n/a
28	chr16:75964393-75964443	Jurkat	blood:	n/a
29	chr16:75964393-75964443	T-47D	breast:	n/a
30	chr16:75964393-75964443	HL-60	blood:	n/a
31	chr16:75964393-75964443	HNPCEpiC	eye:	n/a
32	chr16:75964393-75964443	GM19239	blood:	n/a
33	chr16:75964393-75964443	GM12891	blood:	n/a
34	chr16:75964393-75964443	AoSMC	blood vessel:	n/a
35	chr16:75964393-75964443	RPTEC	kidney:	n/a
36	chr16:75964393-75964443	Hela-S3	cervix:	n/a
37	chr16:75964393-75964443	ProgFib	skin:	n/a
38	chr16:75964393-75964443	HRCEpiC	kidney:	n/a
39	chr16:75964393-75964443	NT2-D1	testis:	n/a
40	chr16:75964393-75964443	GM06990	blood:	n/a
41	chr16:75964393-75964443	NHDF-neo	bronchial:	n/a
42	chr16:75964393-75964443	AG09309	skin:	n/a
43	chr16:75964393-75964443	SKMC	muscle:	n/a
44	chr16:75964393-75964443	NB4	blood:	n/a
45	chr16:75964393-75964443	NH-A	brain:	n/a
46	chr16:75964393-75964443	HMEC	breast:	n/a
47	chr16:75964393-75964443	HRPEpiC	eye:	n/a
48	chr16:75964393-75964443	SK-N-SH	brain:	n/a
49	chr16:75964393-75964443	PANC-1	pancreas:	n/a
50	chr16:75964393-75964443	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:75977745..75979693-chr16:75980372..75982208,2	MCF-7	breast:
2	chr1:90287489..90288189-chr16:75942151..75942717,2	MCF-7	breast:
3	chr16:75905192..75908062-chr16:75922161..75923851,2	K562	blood:
4	chr16:75902948..75904497-chr16:75904944..75907601,2	K562	blood:
5	chr16:75967179..75969484-chr17:4845937..4847850,2	MCF-7	breast:
6	chr16:75962160..75963903-chr16:75968199..75970527,2	K562	blood:
7	chr16:75902948..75904497-chr16:75904944..75907601,2	K562	blood:
8	chr16:75977745..75979693-chr16:75980372..75982208,2	MCF-7	breast:
9	chr16:75962160..75963903-chr16:75968199..75970527,2	K562	blood:
10	chr16:75963255..75965166-chr16:75978260..75980431,2	K562	blood:
11	chr16:75905192..75908062-chr16:75922161..75923851,2	K562	blood:
12	chr16:75963255..75965166-chr16:75978260..75980431,2	K562	blood:

Variant related genes	Relation type
RNA5SP430	TF binding region
ENSG00000261313	TF binding region
RNA5SP430	CpG island
ENSG00000261313	CpG island
ENSG00000108523	chromatin interactions

Extended variants
information (count: 6189 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:6189 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4262972	chr16:75898641-75898642	Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573053953	chr16:75898686-75898687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74442105	chr16:75898694-75898695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76282227	chr16:75898713-75898714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs8047559	chr16:75898714-75898715	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs114539537	chr16:75898755-75898756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560831762	chr16:75898767-75898768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567387069	chr16:75898775-75898776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571405969	chr16:75898782-75898783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs8053897	chr16:75898791-75898792	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs386792205	chr16:75898810-75898811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12103049	chr16:75898821-75898822	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs8047752	chr16:75898832-75898833	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs558275606	chr16:75898834-75898835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532549574	chr16:75898858-75898859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184686170	chr16:75898864-75898865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569202218	chr16:75898894-75898895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs151271688	chr16:75898904-75898905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140635701	chr16:75898929-75898930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535988679	chr16:75898934-75898935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74371347	chr16:75898941-75898942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368641960	chr16:75898989-75898990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376818223	chr16:75899016-75899017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189444124	chr16:75899037-75899038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566343381	chr16:75899048-75899049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569453340	chr16:75899052-75899053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs8050008	chr16:75899070-75899071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs8048260	chr16:75899095-75899096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558894073	chr16:75899224-75899225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370409329	chr16:75899299-75899300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578215556	chr16:75899331-75899332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543882836	chr16:75899335-75899336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554523809	chr16:75899358-75899359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371898140	chr16:75899364-75899365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141234421	chr16:75899428-75899429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553381011	chr16:75899442-75899443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540355061	chr16:75899492-75899493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6564290	chr16:75899508-75899509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532611722	chr16:75899557-75899558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138946779	chr16:75899560-75899561	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs201969738	chr16:75899579-75899580	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs200716163	chr16:75899581-75899582	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs67902461	chr16:75899582-75899583	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs201560837	chr16:75899583-75899584	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs562852038	chr16:75899601-75899602	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs202161045	chr16:75899637-75899638	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs531997443	chr16:75899641-75899642	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs149393288	chr16:75899642-75899643	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs144808955	chr16:75899654-75899655	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs371962017	chr16:75899663-75899664	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75894800-75901600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr16:75894800-75902000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:75896000-75901800	Weak transcription	Brain Anterior Caudate	brain
4	chr16:75896000-75902000	Weak transcription	Brain Angular Gyrus	brain
5	chr16:75896200-75901800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr16:75896200-75901800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr16:75896200-75902000	Weak transcription	Brain Substantia Nigra	brain
8	chr16:75896200-75902200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr16:75897800-75901600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr16:75897800-75901600	Weak transcription	Brain Hippocampus Middle	brain
11	chr16:75901000-75902800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr16:75901600-75902600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr16:75901600-75903000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr16:75901600-75903000	Enhancers	Brain Hippocampus Middle	brain
15	chr16:75901600-75903800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr16:75901600-75903800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr16:75901800-75902800	Enhancers	Brain Cingulate Gyrus	brain
18	chr16:75901800-75903600	Enhancers	Brain Anterior Caudate	brain
19	chr16:75901800-75903800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr16:75902000-75902800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr16:75902000-75903000	Enhancers	Brain Angular Gyrus	brain
22	chr16:75902000-75903400	Enhancers	Brain Substantia Nigra	brain
23	chr16:75902200-75902800	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr16:75902400-75902800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr16:75916400-75917000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr16:75916400-75917000	Enhancers	HepG2	liver
27	chr16:75916400-75917200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr16:75916600-75917000	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr16:75916600-75917400	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr16:75936800-75937400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr16:75937000-75938200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr16:75937000-75938200	Enhancers	HMEC	breast
33	chr16:75937200-75938000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr16:75937600-75938200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr16:75937800-75938200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr16:75938000-75943200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr16:75938200-75943000	Weak transcription	HMEC	breast
38	chr16:75942600-75943400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr16:75942800-75943200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr16:75942800-75943200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr16:75942800-75943400	Enhancers	H1 Cell Line	embryonic stem cell
42	chr16:75942800-75943400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr16:75942800-75943400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr16:75942800-75944000	Enhancers	H9 Cell Line	embryonic stem cell
45	chr16:75943000-75943400	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr16:75943000-75944800	Enhancers	HMEC	breast
47	chr16:75943200-75944600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr16:75944800-75946000	Weak transcription	HMEC	breast
49	chr16:75945800-75946400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr16:75946000-75946200	Enhancers	HMEC	breast

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