Variant report

Variant	esv3401883
Chromosome Location	chr14:56584049-56586947
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:391)
CpG islands
(count:673)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:56584490-56585294	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr14:56585687-56585943	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:56584494-56585224	K562	blood:	n/a	n/a
4	BHLHE40	chr14:56584983-56585142	HepG2	liver:	n/a	n/a
5	CCNT2	chr14:56584668-56585232	K562	blood:	n/a	n/a
6	CCNT2	chr14:56585631-56586108	K562	blood:	n/a	chr14:56585759-56585768
7	CEBPB	chr14:56586857-56587023	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr14:56584703-56584919	Hela-S3	cervix:	n/a	n/a
9	CHD1	chr14:56584405-56584462	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD1	chr14:56586123-56586603	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr14:56585123-56585203	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr14:56585623-56586040	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr14:56584595-56585217	Hela-S3	cervix:	n/a	n/a
14	CREB1	chr14:56584394-56585341	A549	lung:	n/a	n/a
15	CTBP2	chr14:56584489-56586565	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr14:56584960-56585110	K562	blood:	n/a	n/a
17	CTCF	chr14:56584320-56584470	AG04450	lung:	n/a	n/a
18	CTCF	chr14:56585100-56585250	SAEC	small airway:	n/a	n/a
19	CTCF	chr14:56584431-56584491	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr14:56585040-56585190	GM12875	blood:	n/a	n/a
21	CTCF	chr14:56585040-56585190	AG09319	gingival:	n/a	n/a
22	CTCF	chr14:56585616-56585694	GM10266	blood:	n/a	n/a
23	CTCF	chr14:56585008-56585195	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr14:56585040-56585190	Caco-2	colon:	n/a	n/a
25	CTCF	chr14:56586000-56586150	GM12869	blood:	n/a	n/a
26	CTCF	chr14:56586060-56586210	AG04449	skin:	n/a	n/a
27	CTCF	chr14:56585040-56585190	GM06990	blood:	n/a	n/a
28	CTCF	chr14:56585020-56585170	AG09319	gingival:	n/a	n/a
29	CTCF	chr14:56585040-56585190	HPF	lung:	n/a	n/a
30	CTCF	chr14:56584420-56584570	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr14:56586760-56586910	AG10803	skin:	n/a	n/a
32	CTCF	chr14:56585020-56585170	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr14:56585000-56585150	HRE	kidney:	n/a	n/a
34	CTCF	chr14:56585020-56585170	WI-38	lung:	n/a	n/a
35	CTCF	chr14:56585637-56585677	GM19239	blood:	n/a	n/a
36	CTCF	chr14:56584600-56584750	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr14:56585032-56585277	K562	blood:	n/a	n/a
38	CTCF	chr14:56585000-56585150	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr14:56586040-56586190	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr14:56585020-56585170	GM12871	blood:	n/a	n/a
41	CTCF	chr14:56586086-56586097	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr14:56585612-56585724	GM12878	blood:	n/a	n/a
43	CTCF	chr14:56585000-56585150	RPTEC	kidney:	n/a	n/a
44	CTCF	chr14:56585040-56585190	GM12869	blood:	n/a	n/a
45	CTCF	chr14:56585089-56585163	GM12892	blood:	n/a	n/a
46	CTCF	chr14:56584960-56585110	A549	lung:	n/a	n/a
47	CTCF	chr14:56586020-56586170	BJ	skin:	n/a	n/a
48	CTCF	chr14:56584547-56584626	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:56584400-56584550	AG09319	gingival:	n/a	n/a
50	CTCF	chr14:56585040-56585190	HCPEpiC	choroid plexus:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:56586572-56586622	GM12892	blood:	n/a
2	chr14:56584874-56584924	Hela-S3	cervix:	n/a
3	chr14:56586572-56586622	GM12892	blood:	n/a
4	chr14:56584874-56584924	Hela-S3	cervix:	n/a
5	chr14:56585486-56585536	AG09309	skin:	n/a
6	chr14:56584987-56585037	ovcar-3	ovarian:	n/a
7	chr14:56584987-56585037	SK-N-SH_RA	brain:	n/a
8	chr14:56586572-56586622	SKMC	muscle:	n/a
9	chr14:56585102-56585152	HAEpiC	amniotic membrane:	n/a
10	chr14:56584485-56584535	GM12891	blood:	n/a
11	chr14:56584485-56584535	NB4	blood:	n/a
12	chr14:56585486-56585536	ProgFib	skin:	n/a
13	chr14:56586522-56586572	HRPEpiC	eye:	n/a
14	chr14:56585092-56585142	HEK293	kidney:	embryo
15	chr14:56585102-56585152	NB4	blood:	n/a
16	chr14:56586522-56586572	Hela-S3	cervix:	n/a
17	chr14:56585486-56585536	HPAEpiC	pulmonary alveolar:	n/a
18	chr14:56584702-56584752	Caco-2	colon:	n/a
19	chr14:56584647-56584697	AG09309	skin:	n/a
20	chr14:56586028-56586078	K562	blood:	n/a
21	chr14:56584874-56584924	SKMC	muscle:	n/a
22	chr14:56584874-56584924	LNCaP	prostate:	n/a
23	chr14:56584874-56584924	HCPEpiC	choroid plexus:	n/a
24	chr14:56586572-56586622	HEK293	kidney:	embryo
25	chr14:56586572-56586622	Hela-S3	cervix:	n/a
26	chr14:56584987-56585037	GM12891	blood:	n/a
27	chr14:56585486-56585536	Hepatocyte	liver:	n/a
28	chr14:56584874-56584924	HCF	heart:	n/a
29	chr14:56585486-56585536	HL-60	blood:	n/a
30	chr14:56584874-56584924	ovcar-3	ovarian:	n/a
31	chr14:56584987-56585037	MCF10A-Er-Src	breast:	n/a
32	chr14:56584647-56584697	ProgFib	skin:	n/a
33	chr14:56586028-56586078	ProgFib	skin:	n/a
34	chr14:56586522-56586572	Caco-2	colon:	n/a
35	chr14:56584987-56585037	HMEC	breast:	n/a
36	chr14:56585092-56585142	NHBE	bronchial:	n/a
37	chr14:56586522-56586572	NHBE	bronchial:	n/a
38	chr14:56584874-56584924	AG10803	skin:	n/a
39	chr14:56585102-56585152	PANC-1	pancreas:	n/a
40	chr14:56585486-56585536	H1-hESC	embryonic stem cell:	embryo
41	chr14:56585102-56585152	SK-N-SH	brain:	n/a
42	chr14:56586522-56586572	HPAEpiC	pulmonary alveolar:	n/a
43	chr14:56585092-56585142	PANC-1	pancreas:	n/a
44	chr14:56585486-56585536	AG04450	lung:	fetal
45	chr14:56585092-56585142	NT2-D1	testis:	n/a
46	chr14:56586522-56586572	HRCEpiC	kidney:	n/a
47	chr14:56585102-56585152	GM12892	blood:	n/a
48	chr14:56584702-56584752	GM12891	blood:	n/a
49	chr14:56584647-56584697	HMEC	breast:	n/a
50	chr14:56584874-56584924	NT2-D1	testis:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:56582513..56585426-chr14:56585434..56588675,3	K562	blood:
2	chr14:56582513..56585426-chr14:56585434..56588675,3	K562	blood:

No data

Variant related genes	Relation type
PELI2	TF binding region
PELI2	CpG island
ENSG00000139946	chromatin interactions

Extended variants
information (count: 133 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144494194	chr14:56584055-56584056	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs3850295	chr14:56584091-56584092	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs34526272	chr14:56584164-56584165	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs202207226	chr14:56584168-56584169	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs35894411	chr14:56584169-56584170	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs199785651	chr14:56584171-56584172	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs398057114	chr14:56584172-56584173	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs183772361	chr14:56584190-56584191	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs574391111	chr14:56584192-56584193	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs147836390	chr14:56584197-56584198	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs370909292	chr14:56584233-56584234	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs75047388	chr14:56584254-56584255	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs572201429	chr14:56584264-56584265	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs141325729	chr14:56584266-56584267	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs567482743	chr14:56584297-56584298	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs188130499	chr14:56584358-56584359	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs368958888	chr14:56584391-56584392	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs577259075	chr14:56584398-56584399	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs546011636	chr14:56584416-56584417	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs576354685	chr14:56584451-56584452	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs371956788	chr14:56584454-56584455	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs3186565	chr14:56584499-56584500	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs564865685	chr14:56584528-56584529	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs117160902	chr14:56584544-56584545	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs1046596	chr14:56584561-56584562	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs370718352	chr14:56584564-56584565	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs35010696	chr14:56584566-56584567	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs530014207	chr14:56584585-56584586	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs146571783	chr14:56584617-56584618	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs1046597	chr14:56584625-56584626	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs61737286	chr14:56584649-56584650	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376436624	chr14:56584664-56584665	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs375038795	chr14:56584665-56584666	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs368832906	chr14:56584730-56584731	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs3742572	chr14:56584804-56584805	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs552624041	chr14:56584806-56584807	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs187295432	chr14:56584812-56584813	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs372188672	chr14:56584820-56584821	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs3742573	chr14:56584837-56584838	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs566287560	chr14:56584868-56584869	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs535124101	chr14:56584876-56584877	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs546638384	chr14:56584883-56584884	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs568483006	chr14:56584886-56584887	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs536549628	chr14:56584896-56584897	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs554934622	chr14:56584917-56584918	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs111534123	chr14:56585009-56585010	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs576290908	chr14:56585066-56585067	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs537211485	chr14:56585075-56585076	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs558736919	chr14:56585122-56585123	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs576815227	chr14:56585125-56585126	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
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
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
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56579800-56584200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr14:56582000-56584200	Enhancers	Primary T cells from cord blood	blood
3	chr14:56582000-56584200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:56582000-56584200	Enhancers	Fetal Brain Male	brain
5	chr14:56582200-56584200	Enhancers	Fetal Thymus	thymus
6	chr14:56582200-56584600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr14:56582400-56584200	Enhancers	Dnd41	blood
8	chr14:56582600-56584200	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr14:56582600-56584200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr14:56582600-56584400	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr14:56582600-56584400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr14:56582600-56584600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr14:56582800-56584200	Enhancers	Primary T cells fromperipheralblood	blood
14	chr14:56582800-56584200	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr14:56582800-56584200	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr14:56582800-56584200	Enhancers	Fetal Lung	lung
17	chr14:56583000-56584200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:56583000-56584200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr14:56583000-56584200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr14:56583000-56584200	Enhancers	Brain Hippocampus Middle	brain
21	chr14:56583000-56584800	Flanking Active TSS	Primary B cells from cord blood	blood
22	chr14:56583200-56584200	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr14:56583200-56584200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr14:56583200-56584200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr14:56583200-56584200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr14:56583200-56584200	Enhancers	Adipose Nuclei	Adipose
27	chr14:56583200-56584200	Enhancers	Brain Cingulate Gyrus	brain
28	chr14:56583200-56584200	Enhancers	Fetal Intestine Small	intestine
29	chr14:56583200-56584400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr14:56583200-56584800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr14:56583400-56584200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr14:56583400-56584200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr14:56583400-56584200	Enhancers	Fetal Kidney	kidney
34	chr14:56583400-56584200	Weak transcription	Thymus	Thymus
35	chr14:56583400-56584400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr14:56583400-56584400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr14:56583400-56584400	Weak transcription	Psoas Muscle	Psoas
38	chr14:56583400-56587600	Active TSS	Ovary	ovary
39	chr14:56583600-56584200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr14:56583600-56584200	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr14:56583600-56584400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr14:56583600-56584400	Weak transcription	Gastric	stomach
43	chr14:56583600-56584400	Weak transcription	Lung	lung
44	chr14:56583600-56584400	Weak transcription	Pancreas	Pancrea
45	chr14:56583600-56584400	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr14:56583800-56584200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
47	chr14:56583800-56584200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr14:56583800-56584200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr14:56583800-56584200	Enhancers	Liver	Liver
50	chr14:56583800-56584200	Enhancers	Brain Substantia Nigra	brain

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