Variant report

Variant	nsv563853
Chromosome Location	chr14:22242293-22292805
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	CEBPB	chr14:22270575-22270843	HepG2	liver:	n/a	chr14:22270690-22270701
2	CEBPB	chr14:22249065-22249134	HepG2	liver:	n/a	n/a
3	CEBPB	chr14:22249926-22250066	HepG2	liver:	n/a	n/a
4	CEBPB	chr14:22278968-22279088	HepG2	liver:	n/a	chr14:22279034-22279045
5	CTCF	chr14:22255646-22255739	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr14:22265200-22265320	HUVEC	blood vessel:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
7	CTCF	chr14:22265184-22265375	NHEK	skin:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
8	CTCF	chr14:22265220-22265370	GM12871	blood:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
9	CTCF	chr14:22265260-22265410	HRPEpiC	eye:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
10	CTCF	chr14:22265120-22265270	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr14:22261700-22261850	NHLF	lung:	n/a	n/a
12	CTCF	chr14:22265180-22265330	Hela-S3	cervix:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
13	CTCF	chr14:22265248-22265308	Gliobla	brain:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
14	CTCF	chr14:22265220-22265370	MCF-7	breast:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
15	CTCF	chr14:22276288-22276391	K562	blood:	n/a	chr14:22276320-22276336 chr14:22276319-22276337 chr14:22276321-22276334 chr14:22276321-22276334
16	CTCF	chr14:22265140-22265290	A549	lung:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
17	CTCF	chr14:22265200-22265350	GM12864	blood:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
18	CTCF	chr14:22256980-22257130	MCF-7	breast:	n/a	n/a
19	CTCF	chr14:22272220-22272370	K562	blood:	n/a	n/a
20	CTCF	chr14:22265215-22265324	HepG2	liver:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
21	CTCF	chr14:22251940-22252090	HepG2	liver:	n/a	n/a
22	CTCF	chr14:22276200-22276350	GM12874	blood:	n/a	chr14:22276320-22276336 chr14:22276319-22276337 chr14:22276321-22276334 chr14:22276321-22276334
23	CTCF	chr14:22269697-22269729	GM10248	blood:	n/a	n/a
24	CTCF	chr14:22265180-22265330	GM12864	blood:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
25	CTCF	chr14:22265076-22265457	MCF-7	breast:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
26	CTCF	chr14:22265220-22265370	HRE	kidney:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
27	CTCF	chr14:22245025-22245061	Lung_OC	lung:	n/a	n/a
28	CTCF	chr14:22256920-22257070	HEK293	kidney:	n/a	n/a
29	CTCF	chr14:22256920-22257070	HVMF	connective:	n/a	n/a
30	CTCF	chr14:22265220-22265370	HPAF	blood vessel:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
31	CTCF	chr14:22265180-22265330	HAc	cerebellar:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
32	CTCF	chr14:22265168-22265335	K562	blood:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
33	CTCF	chr14:22276280-22276430	HepG2	liver:	n/a	chr14:22276320-22276336 chr14:22276319-22276337 chr14:22276321-22276334 chr14:22276321-22276334
34	CTCF	chr14:22265172-22265358	LNCaP	prostate:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
35	CTCF	chr14:22256920-22257070	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:22265160-22265310	GM12864	blood:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
37	CTCF	chr14:22265240-22265390	GM12872	blood:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
38	CTCF	chr14:22256920-22257070	A549	lung:	n/a	n/a
39	CTCF	chr14:22265221-22265301	K562	blood:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
40	CTCF	chr14:22265300-22265450	HMF	breast:	n/a	n/a
41	CTCF	chr14:22265201-22265336	A549	lung:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
42	CTCF	chr14:22265220-22265370	HMEC	breast:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
43	CTCF	chr14:22265140-22265290	HEK293	kidney:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
44	CTCF	chr14:22276165-22276410	H1-hESC	embryonic stem cell:	n/a	chr14:22276320-22276336 chr14:22276319-22276337 chr14:22276321-22276334 chr14:22276321-22276334
45	CTCF	chr14:22265120-22265270	NHEK	skin:	n/a	n/a
46	CTCF	chr14:22265164-22265372	MCF-7	breast:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
47	CTCF	chr14:22265140-22265290	HA-sp	spinal cord:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
48	CTCF	chr14:22265220-22265370	HBMEC	blood vessel:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
49	CTCF	chr14:22265180-22265330	HCPEpiC	choroid plexus:	n/a	chr14:22265262-22265283 chr14:22265260-22265278
50	CTCF	chr14:22265189-22265357	MCF-7	breast:	n/a	chr14:22265262-22265283 chr14:22265260-22265278

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22279816-22279866	HAEpiC	amniotic membrane:	n/a
2	chr14:22279816-22279866	HAEpiC	amniotic membrane:	n/a
3	chr14:22265369-22265419	HRCEpiC	kidney:	n/a
4	chr14:22279816-22279866	HCF	heart:	n/a
5	chr14:22292347-22292397	HCPEpiC	choroid plexus:	n/a
6	chr14:22292347-22292397	AoSMC	blood vessel:	n/a
7	chr14:22265369-22265419	Hela-S3	cervix:	n/a
8	chr14:22265369-22265419	GM12878	blood:	n/a
9	chr14:22279816-22279866	Hela-S3	cervix:	n/a
10	chr14:22292347-22292397	T-47D	breast:	n/a
11	chr14:22265369-22265419	HRE	kidney:	n/a
12	chr14:22265369-22265419	SK-N-SH_RA	brain:	n/a
13	chr14:22292347-22292397	HepG2	liver:	n/a
14	chr14:22265369-22265419	GM12892	blood:	n/a
15	chr14:22265369-22265419	NB4	blood:	n/a
16	chr14:22279816-22279866	SKMC	muscle:	n/a
17	chr14:22292347-22292397	NB4	blood:	n/a
18	chr14:22279816-22279866	SAEC	small airway:	n/a
19	chr14:22279816-22279866	U87	brain:	n/a
20	chr14:22279816-22279866	BE2_C	brain:	n/a
21	chr14:22279816-22279866	NT2-D1	testis:	n/a
22	chr14:22292347-22292397	HIPEpiC	eye:	n/a
23	chr14:22265369-22265419	HNPCEpiC	eye:	n/a
24	chr14:22292347-22292397	GM19239	blood:	n/a
25	chr14:22279816-22279866	Jurkat	blood:	n/a
26	chr14:22279816-22279866	A549	lung:	n/a
27	chr14:22265369-22265419	Jurkat	blood:	n/a
28	chr14:22279816-22279866	AoSMC	blood vessel:	n/a
29	chr14:22265369-22265419	AG09309	skin:	n/a
30	chr14:22292347-22292397	NT2-D1	testis:	n/a
31	chr14:22292347-22292397	U87	brain:	n/a
32	chr14:22279816-22279866	NHBE	bronchial:	n/a
33	chr14:22279816-22279866	GM06990	blood:	n/a
34	chr14:22279816-22279866	NHDF-neo	bronchial:	n/a
35	chr14:22292347-22292397	GM12891	blood:	n/a
36	chr14:22279816-22279866	SK-N-SH	brain:	n/a
37	chr14:22279816-22279866	HPAEpiC	pulmonary alveolar:	n/a
38	chr14:22292347-22292397	HCF	heart:	n/a
39	chr14:22265369-22265419	SK-N-MC	brain:	n/a
40	chr14:22292347-22292397	AG09309	skin:	n/a
41	chr14:22279816-22279866	GM12878	blood:	n/a
42	chr14:22292347-22292397	HL-60	blood:	n/a
43	chr14:22279816-22279866	NB4	blood:	n/a
44	chr14:22292347-22292397	K562	blood:	n/a
45	chr14:22279816-22279866	ProgFib	skin:	n/a
46	chr14:22292347-22292397	BJ	skin:	n/a
47	chr14:22265369-22265419	HUVEC	blood vessel:	n/a
48	chr14:22265369-22265419	BE2_C	brain:	n/a
49	chr14:22265369-22265419	NT2-D1	testis:	n/a
50	chr14:22292347-22292397	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr14:22256716..22259521-chr14:22263376..22264997,2	MCF-7	breast:
2	chr14:22264815..22265316-chr14:22293406..22294027,2	MCF-7	breast:
3	chr14:22238003..22239945-chr14:22252615..22254697,2	MCF-7	breast:
4	chr14:22256716..22259521-chr14:22263376..22264997,2	MCF-7	breast:

Variant related genes	Relation type
TRAV8-1	TF binding region
ENSG00000222776	TF binding region
TRAV7	TF binding region
TRAV10	TF binding region
TRAV11	TF binding region
TRAV9-1	TF binding region
TRAV8-1	CpG island
ENSG00000222776	CpG island
TRAV7	CpG island
TRAV10	CpG island
TRAV11	CpG island
TRAV9-1	CpG island
ENSG00000211784	chromatin interactions

Extended variants
information (count: 798 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:798 , 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	rs4982506	chr14:22242293-22242294	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561532118	chr14:22242295-22242296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112854313	chr14:22242306-22242307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4246993	chr14:22242339-22242340	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs143109669	chr14:22242399-22242400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376923082	chr14:22242407-22242408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117292328	chr14:22242426-22242427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538901266	chr14:22242432-22242433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551450395	chr14:22242464-22242465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184205589	chr14:22242513-22242514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78933275	chr14:22242528-22242529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556552411	chr14:22242533-22242534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573331919	chr14:22242599-22242600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377280495	chr14:22242617-22242618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188962343	chr14:22242632-22242633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4982507	chr14:22242646-22242647	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs551143415	chr14:22242679-22242680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544879901	chr14:22242717-22242718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199631145	chr14:22242737-22242738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs578128848	chr14:22242763-22242764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181187974	chr14:22242770-22242771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148273059	chr14:22242790-22242791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544589620	chr14:22242806-22242807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561244554	chr14:22242837-22242838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs17182796	chr14:22242839-22242840	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs547303495	chr14:22242885-22242886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs72689736	chr14:22242888-22242889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs555794040	chr14:22242890-22242891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373460435	chr14:22242901-22242902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4981379	chr14:22242931-22242932	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs77472608	chr14:22242933-22242934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538216070	chr14:22242940-22242941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536729769	chr14:22242961-22242962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575053957	chr14:22242962-22242963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184675253	chr14:22242973-22242974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189945622	chr14:22243045-22243046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535893270	chr14:22243075-22243076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553186184	chr14:22243088-22243089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145549863	chr14:22243089-22243090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538792381	chr14:22243093-22243094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558494730	chr14:22243122-22243123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561357181	chr14:22243165-22243166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs180839366	chr14:22243167-22243168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531561628	chr14:22243192-22243193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73580246	chr14:22243228-22243229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs544702050	chr14:22243280-22243281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561407005	chr14:22243284-22243285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574881811	chr14:22243314-22243315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4982508	chr14:22243421-22243422	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs34217908	chr14:22243496-22243497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Barrett''s syndrome	19417022	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22237000-22244600	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr14:22237400-22245000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:22240000-22244600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr14:22244400-22245400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr14:22244400-22245600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr14:22244600-22245400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr14:22244600-22245400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr14:22244800-22245600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr14:22245000-22245200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr14:22245200-22245800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr14:22245400-22248600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr14:22245400-22248600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr14:22245400-22248600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr14:22245800-22246200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr14:22246200-22246400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr14:22246400-22246800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr14:22248600-22248800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr14:22248600-22248800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
19	chr14:22248600-22248800	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr14:22248600-22248800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr14:22248600-22249000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr14:22248800-22249000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr14:22248800-22249200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr14:22249000-22249200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr14:22249200-22250200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr14:22250000-22250200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr14:22261600-22262000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chr14:22263200-22263400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
29	chr14:22263400-22265200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr14:22265000-22265400	Active TSS	Thymus	Thymus
31	chr14:22265200-22265600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
32	chr14:22265400-22265800	Enhancers	Brain Anterior Caudate	brain
33	chr14:22265400-22265800	Flanking Active TSS	Thymus	Thymus
34	chr14:22265400-22266000	Active TSS	Primary T cells fromperipheralblood	blood
35	chr14:22265400-22266000	Enhancers	Fetal Thymus	thymus
36	chr14:22265600-22266000	Active TSS	Primary T regulatory cells fromperipheralblood	blood
37	chr14:22265800-22267600	Active TSS	Thymus	Thymus
38	chr14:22269800-22270000	Enhancers	Brain Substantia Nigra	brain
39	chr14:22270000-22270600	Weak transcription	Brain Substantia Nigra	brain
40	chr14:22270400-22270800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr14:22270400-22271200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr14:22270400-22271200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr14:22270600-22271000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr14:22270600-22271000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr14:22270600-22271000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr14:22270600-22271000	Active TSS	Brain Substantia Nigra	brain
47	chr14:22270800-22271200	Enhancers	H1 Cell Line	embryonic stem cell
48	chr14:22270800-22271400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr14:22271000-22271400	Enhancers	Brain Substantia Nigra	brain
50	chr14:22271600-22274000	Enhancers	Primary neutrophils fromperipheralblood	blood

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