Variant report

Variant	nsv901479
Chromosome Location	chr14:22102800-22146832
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	ATF1	chr14:22109400-22109600	K562	blood:	n/a	n/a
2	BACH1	chr14:22143914-22143985	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr14:22115304-22115582	A549	lung:	n/a	chr14:22115409-22115422 chr14:22115409-22115420 chr14:22115409-22115422 chr14:22115409-22115422 chr14:22115411-22115422
4	CEBPB	chr14:22124752-22125048	K562	blood:	n/a	chr14:22124889-22124900
5	CEBPB	chr14:22131065-22131322	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:22126294-22126423	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr14:22107189-22107485	HepG2	liver:	n/a	chr14:22107316-22107327
8	CEBPB	chr14:22131129-22131312	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr14:22115230-22115604	MCF-7	breast:	n/a	chr14:22115409-22115422 chr14:22115409-22115420 chr14:22115409-22115422 chr14:22115409-22115422 chr14:22115411-22115422
10	CEBPB	chr14:22115287-22115570	K562	blood:	n/a	chr14:22115409-22115422 chr14:22115409-22115420 chr14:22115409-22115422 chr14:22115409-22115422 chr14:22115411-22115422
11	CEBPB	chr14:22115279-22115699	MCF-7	breast:	n/a	chr14:22115409-22115422 chr14:22115409-22115420 chr14:22115409-22115422 chr14:22115409-22115422 chr14:22115411-22115422
12	CEBPB	chr14:22126297-22126473	A549	lung:	n/a	n/a
13	CEBPB	chr14:22115274-22115574	HepG2	liver:	n/a	chr14:22115409-22115422 chr14:22115409-22115420 chr14:22115409-22115422 chr14:22115409-22115422 chr14:22115411-22115422
14	CEBPB	chr14:22131108-22131332	IMR90	lung:	n/a	n/a
15	CEBPB	chr14:22126286-22126507	HepG2	liver:	n/a	n/a
16	CEBPB	chr14:22124782-22125029	IMR90	lung:	n/a	chr14:22124889-22124900
17	CEBPB	chr14:22124746-22125041	HepG2	liver:	n/a	chr14:22124889-22124900
18	CTCF	chr14:22109520-22109670	BE2_C	brain:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
19	CTCF	chr14:22109439-22109625	A549	lung:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
20	CTCF	chr14:22109420-22109570	HEK293	kidney:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
21	CTCF	chr14:22109416-22109627	MCF-7	breast:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
22	CTCF	chr14:22109361-22109722	GM12878	blood:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
23	CTCF	chr14:22109427-22109610	K562	blood:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
24	CTCF	chr14:22109148-22109866	A549	lung:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
25	CTCF	chr14:22109460-22109610	HMF	breast:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
26	CTCF	chr14:22109480-22109630	Hela-S3	cervix:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
27	CTCF	chr14:22109459-22109626	Lung_OC	lung:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
28	CTCF	chr14:22109420-22109570	Hela-S3	cervix:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
29	CTCF	chr14:22109414-22109635	MCF-7	breast:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
30	CTCF	chr14:22109520-22109670	MCF-7	breast:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
31	CTCF	chr14:22109460-22109610	HCFaa	heart:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
32	CTCF	chr14:22109400-22109592	K562	blood:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
33	CTCF	chr14:22109480-22109630	HPAF	blood vessel:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
34	CTCF	chr14:22109420-22109570	GM12873	blood:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
35	CTCF	chr14:22109360-22109510	HCT-116	colon:	n/a	n/a
36	CTCF	chr14:22109420-22109570	GM12865	blood:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
37	CTCF	chr14:22109420-22109570	HRPEpiC	eye:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
38	CTCF	chr14:22109120-22109270	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr14:22115809-22115811	LNCaP	prostate:	n/a	n/a
40	CTCF	chr14:22122644-22122696	GM12891	blood:	n/a	n/a
41	CTCF	chr14:22109440-22109590	GM12868	blood:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
42	CTCF	chr14:22109407-22109668	LNCaP	prostate:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
43	CTCF	chr14:22109480-22109630	HAc	cerebellar:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
44	CTCF	chr14:22122578-22122690	GM19239	blood:	n/a	n/a
45	CTCF	chr14:22109500-22109650	RPTEC	kidney:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
46	CTCF	chr14:22109420-22109570	SK-N-SH_RA	brain:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
47	CTCF	chr14:22109480-22109630	GM12872	blood:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
48	CTCF	chr14:22109520-22109750	SAEC	small airway:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
49	CTCF	chr14:22109466-22109582	ProgFib	skin:	n/a	chr14:22109539-22109560 chr14:22109537-22109555
50	CTCF	chr14:22109460-22109610	GM12864	blood:	n/a	chr14:22109539-22109560 chr14:22109537-22109555

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22103310-22103360	SKMC	muscle:	n/a
2	chr14:22110278-22110328	IMR90	lung:	fetal
3	chr14:22103082-22103132	HMEC	breast:	n/a
4	chr14:22131976-22132026	PrEC	prostate:	n/a
5	chr14:22133789-22133839	GM12878	blood:	n/a
6	chr14:22103031-22103081	HIPEpiC	eye:	n/a
7	chr14:22103031-22103081	HEEpiC	esophagus:	n/a
8	chr14:22103504-22103554	A549	lung:	n/a
9	chr14:22103082-22103132	AG09309	skin:	n/a
10	chr14:22133789-22133839	HAEpiC	amniotic membrane:	n/a
11	chr14:22103504-22103554	HMEC	breast:	n/a
12	chr14:22133789-22133839	HCF	heart:	n/a
13	chr14:22103504-22103554	AG09309	skin:	n/a
14	chr14:22133789-22133839	Hepatocyte	liver:	n/a
15	chr14:22133789-22133839	MCF10A-Er-Src	breast:	n/a
16	chr14:22110278-22110328	H1-hESC	embryonic stem cell:	embryo
17	chr14:22103310-22103360	AG04449	skin:	fetal
18	chr14:22103726-22103776	AoSMC	blood vessel:	n/a
19	chr14:22132021-22132071	HCM	heart:	n/a
20	chr14:22103082-22103132	HUVEC	blood vessel:	n/a
21	chr14:22131976-22132026	GM06990	blood:	n/a
22	chr14:22132021-22132071	HIPEpiC	eye:	n/a
23	chr14:22103310-22103360	HCT-116	colon:	n/a
24	chr14:22133789-22133839	CMK	blood:	n/a
25	chr14:22110278-22110328	ECC-1	luminal epithelium:	n/a
26	chr14:22110278-22110328	BJ	skin:	n/a
27	chr14:22131976-22132026	A549	lung:	n/a
28	chr14:22103082-22103132	GM12891	blood:	n/a
29	chr14:22103310-22103360	NHDF-neo	bronchial:	n/a
30	chr14:22103726-22103776	SAEC	small airway:	n/a
31	chr14:22111727-22111777	NT2-D1	testis:	n/a
32	chr14:22133789-22133839	NHBE	bronchial:	n/a
33	chr14:22103031-22103081	AG09319	gingival:	n/a
34	chr14:22103504-22103554	HRCEpiC	kidney:	n/a
35	chr14:22103082-22103132	AG10803	skin:	n/a
36	chr14:22103310-22103360	HCF	heart:	n/a
37	chr14:22111727-22111777	PrEC	prostate:	n/a
38	chr14:22110278-22110328	HCM	heart:	n/a
39	chr14:22133789-22133839	SK-N-MC	brain:	n/a
40	chr14:22103310-22103360	RPTEC	kidney:	n/a
41	chr14:22110278-22110328	MCF-7	breast:	n/a
42	chr14:22133789-22133839	HCM	heart:	n/a
43	chr14:22103031-22103081	GM06990	blood:	n/a
44	chr14:22103082-22103132	AoSMC	blood vessel:	n/a
45	chr14:22111727-22111777	HEK293	kidney:	embryo
46	chr14:22110278-22110328	GM19239	blood:	n/a
47	chr14:22110278-22110328	U87	brain:	n/a
48	chr14:22110278-22110328	AoSMC	blood vessel:	n/a
49	chr14:22103031-22103081	HMEC	breast:	n/a
50	chr14:22110278-22110328	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:22140885..22141748-chr5:66767836..66768488,2	MCF-7	breast:
2	chr14:22025433..22026344-chr14:22109433..22110015,2	MCF-7	breast:
3	chr13:69008871..69009371-chr14:22109098..22109604,2	MCF-7	breast:
4	chr14:22109038..22109779-chr14:22179252..22179808,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR10G2-2	chr14:22117944-22118553	NONHSAT035700

Variant related genes	Relation type
OR4E2	TF binding region
ARL6IP1P1	TF binding region
OR10G2	TF binding region
OR4E1	TF binding region
TRAV1-2	TF binding region
OR4E2	CpG island
ARL6IP1P1	CpG island
OR10G2	CpG island
OR4E1	CpG island
TRAV1-2	CpG island

Extended variants
information (count: 786 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28586589	chr14:22103310-22103311	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529806120	chr14:22103359-22103360	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs371882359	chr14:22103726-22103727	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs117158393	chr14:22105800-22105801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539708429	chr14:22105802-22105803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556217262	chr14:22105804-22105805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569841430	chr14:22105820-22105821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76170896	chr14:22105841-22105842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11850953	chr14:22105880-22105881	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs562064312	chr14:22105914-22105915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572578026	chr14:22105929-22105930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs3926331	chr14:22105963-22105964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541214189	chr14:22105983-22105984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558124721	chr14:22106014-22106015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185593841	chr14:22106021-22106022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112438836	chr14:22106022-22106023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563660343	chr14:22106046-22106047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4982476	chr14:22106048-22106049	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs4981377	chr14:22106074-22106075	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs74034966	chr14:22106079-22106080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527374872	chr14:22106089-22106090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547213636	chr14:22106103-22106104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570409821	chr14:22106182-22106183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12433499	chr14:22106184-22106185	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs188891371	chr14:22106185-22106186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573802501	chr14:22106189-22106190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs369261872	chr14:22106208-22106209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544278450	chr14:22106213-22106214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73588706	chr14:22106221-22106222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138472418	chr14:22106257-22106258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114562536	chr14:22106260-22106261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535102524	chr14:22106296-22106297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117583815	chr14:22106299-22106300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61974099	chr14:22106343-22106344	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs376800068	chr14:22106379-22106380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560373248	chr14:22106380-22106381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs8015955	chr14:22106389-22106390	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs573997543	chr14:22106396-22106397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192254773	chr14:22106416-22106417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566453094	chr14:22106438-22106439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528710854	chr14:22106442-22106443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12892897	chr14:22106500-22106501	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs532902799	chr14:22106513-22106514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs61974100	chr14:22106522-22106523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs61974101	chr14:22106529-22106530	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs144219225	chr14:22106533-22106534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148748246	chr14:22106542-22106543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73588707	chr14:22106548-22106549	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs565847472	chr14:22106549-22106550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549821093	chr14:22106588-22106589	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Autism	22102821	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22105800-22106800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:22106000-22106800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:22107200-22107600	Enhancers	HepG2	liver
4	chr14:22110200-22112000	Active TSS	Primary T cells fromperipheralblood	blood
5	chr14:22110800-22111800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
6	chr14:22111000-22111200	Enhancers	Primary T cells from cord blood	blood
7	chr14:22111000-22111800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
8	chr14:22111000-22112000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr14:22111000-22112000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr14:22111000-22112000	Enhancers	H9 Cell Line	embryonic stem cell
11	chr14:22111000-22112200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr14:22111000-22112200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr14:22111000-22112200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr14:22111000-22112200	Active TSS	Fetal Thymus	thymus
15	chr14:22111200-22112000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr14:22111200-22112000	Active TSS	Primary T cells from cord blood	blood
17	chr14:22111200-22112400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr14:22111400-22111800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr14:22111400-22111800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr14:22111400-22112600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr14:22111600-22111800	Bivalent Enhancer	Hela-S3	cervix
22	chr14:22111600-22112000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr14:22111600-22112200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr14:22115600-22116600	Enhancers	Fetal Brain Male	brain
25	chr14:22120200-22120800	Enhancers	Spleen	Spleen
26	chr14:22120200-22121000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr14:22120200-22121000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:22120200-22122600	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr14:22120400-22120800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr14:22120400-22120800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr14:22120400-22120800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr14:22120400-22120800	Enhancers	HUVEC	blood vessel
33	chr14:22120400-22121000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr14:22120400-22121000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr14:22120400-22121000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr14:22120400-22121000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:22120400-22121000	Enhancers	Lung	lung
38	chr14:22120400-22121200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr14:22120400-22122800	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr14:22120600-22120800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr14:22120600-22120800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr14:22120600-22120800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
43	chr14:22120600-22121000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:22120600-22121000	Enhancers	H9 Cell Line	embryonic stem cell
45	chr14:22120600-22121000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr14:22120600-22121800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr14:22120800-22122400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr14:22121000-22122400	Weak transcription	Lung	lung
49	chr14:22122600-22122800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:22122600-22122800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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