Variant report

Variant	rs11160833
Chromosome Location	chr14:105557054-105557055
allele	C/G
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	MAX	chr14:105556409-105559034	MCF-7	breast:	n/a	chr14:105558119-105558129 chr14:105558711-105558721 chr14:105558880-105558895 chr14:105558887-105558897
2	POLR2A	chr14:105556811-105557139	A549	lung:	n/a	n/a
3	TCF12	chr14:105556669-105559848	ECC-1	luminal epithelium:	n/a	chr14:105558705-105558715 chr14:105556711-105556721 chr14:105558506-105558516 chr14:105558328-105558335 chr14:105556879-105556889 chr14:105556900-105556910 chr14:105558295-105558305 chr14:105557507-105557514
4	NR3C1	chr14:105556692-105557299	A549	lung:	n/a	chr14:105556824-105556833
5	RFX5	chr14:105556832-105557157	Hela-S3	cervix:	n/a	n/a
6	MAX	chr14:105556813-105557175	K562	blood:	n/a	n/a
7	CTCF	chr14:105556920-105557070	NHLF	lung:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
8	MYC	chr14:105556712-105559367	A549	lung:	n/a	chr14:105558119-105558129 chr14:105558711-105558721 chr14:105558880-105558895 chr14:105559297-105559307 chr14:105558887-105558897
9	CTCF	chr14:105556838-105557162	GM12878	blood:	n/a	chr14:105556998-105557011 chr14:105556857-105556866 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
10	CTCF	chr14:105556940-105557090	GM06990	blood:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
11	CTCF	chr14:105556920-105557070	GM12867	blood:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
12	CTCF	chr14:105556960-105557110	GM12868	blood:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
13	BCL3	chr14:105556352-105559650	A549	lung:	n/a	chr14:105559601-105559614 chr14:105558706-105558719 chr14:105559120-105559133
14	CTCF	chr14:105556940-105557090	HCPEpiC	choroid plexus:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
15	CTCF	chr14:105556779-105557139	ECC-1	luminal epithelium:	n/a	chr14:105556805-105556818 chr14:105556998-105557011 chr14:105556857-105556866 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
16	FOXM1	chr14:105556756-105558866	ECC-1	luminal epithelium:	n/a	n/a
17	CTCF	chr14:105556845-105557148	GM10266	blood:	n/a	chr14:105556998-105557011 chr14:105556857-105556866 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
18	RFX5	chr14:105556916-105557068	K562	blood:	n/a	n/a
19	CTCF	chr14:105556920-105557070	NB4	blood:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
20	CTCF	chr14:105556920-105557070	GM12864	blood:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
21	RAD21	chr14:105556813-105557197	Hela-S3	cervix:	n/a	chr14:105556999-105557012 chr14:105556915-105556929 chr14:105556996-105557015 chr14:105556853-105556866 chr14:105557001-105557011
22	RCOR1	chr14:105556835-105557225	Hela-S3	cervix:	n/a	n/a
23	WRNIP1	chr14:105557003-105557086	GM12878	blood:	n/a	n/a
24	ELK1	chr14:105556781-105557077	GM12878	blood:	n/a	n/a
25	YY1	chr14:105556791-105557075	GM12892	blood:	n/a	n/a
26	TBL1XR1	chr14:105556941-105557181	K562	blood:	n/a	n/a
27	CTCF	chr14:105556920-105557070	AG04450	lung:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
28	CTCF	chr14:105556865-105557123	MCF-7	breast:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
29	CTCF	chr14:105556940-105557090	HepG2	liver:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
30	CTCF	chr14:105556920-105557070	WI-38	lung:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
31	SP1	chr14:105556757-105557179	GM12878	blood:	n/a	chr14:105557021-105557030
32	MAX	chr14:105556809-105559855	ECC-1	luminal epithelium:	n/a	chr14:105558119-105558129 chr14:105558711-105558721 chr14:105558880-105558895 chr14:105559297-105559307 chr14:105559437-105559447 chr14:105558887-105558897
33	CTCF	chr14:105556920-105557070	HA-sp	spinal cord:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
34	CTCF	chr14:105556895-105557082	A549	lung:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
35	RAD21	chr14:105556699-105557333	MCF-7	breast:	n/a	chr14:105556999-105557012 chr14:105556915-105556929 chr14:105556996-105557015 chr14:105556853-105556866 chr14:105557001-105557011
36	TCF12	chr14:105552661-105561002	A549	lung:	n/a	chr14:105555506-105555515 chr14:105554733-105554741 chr14:105554099-105554109 chr14:105560562-105560572 chr14:105558705-105558715 chr14:105556711-105556721 chr14:105560974-105560982 chr14:105558506-105558516 chr14:105555994-105556004 chr14:105558328-105558335 chr14:105556609-105556616 chr14:105556879-105556889 chr14:105556900-105556910 chr14:105558295-105558305 chr14:105557507-105557514
37	CTCF	chr14:105556866-105557138	GM10248	blood:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
38	POLR2A	chr14:105556792-105557348	A549	lung:	n/a	n/a
39	TBL1XR1	chr14:105556932-105557132	K562	blood:	n/a	n/a
40	MAZ	chr14:105556890-105557159	HepG2	liver:	n/a	n/a
41	CTCF	chr14:105556761-105557227	H1-hESC	embryonic stem cell:	n/a	chr14:105556805-105556818 chr14:105556998-105557011 chr14:105556857-105556866 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
42	JUND	chr14:105556473-105557234	A549	lung:	n/a	n/a
43	CTCF	chr14:105556940-105557090	GM12869	blood:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
44	CTCF	chr14:105556920-105557070	HMF	breast:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
45	CTCF	chr14:105556940-105557090	HPAF	blood vessel:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
46	NR2F2	chr14:105556798-105557150	K562	blood:	n/a	n/a
47	MAX	chr14:105556897-105557154	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr14:105556920-105557070	SAEC	small airway:	n/a	chr14:105556998-105557011 chr14:105556995-105557013 chr14:105556997-105557018 chr14:105557000-105557010 chr14:105556996-105557012 chr14:105556998-105557011 chr14:105556998-105557007
49	BHLHE40	chr14:105556854-105557157	GM12878	blood:	n/a	n/a
50	POLR2A	chr14:105556836-105557394	HCT-116	colon:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105556568..105557626-chr14:105644344..105645020,4	MCF-7	breast:
2	chr14:105556907..105557905-chr14:105631981..105632717,2	MCF-7	breast:
3	chr14:105556528..105557420-chr14:105633531..105634669,3	MCF-7	breast:
4	chr14:105552947..105555057-chr14:105555509..105557119,2	K562	blood:
5	chr14:105556660..105559437-chr14:105588253..105590015,2	MCF-7	breast:
6	chr14:105556545..105557474-chr14:105818256..105819211,4	K562	blood:
7	chr14:105555328..105560254-chr14:105631379..105635555,5	MCF-7	breast:
8	chr14:105556861..105558363-chr14:105628903..105631842,2	K562	blood:
9	chr14:105556943..105557444-chr17:58513028..58513593,2	MCF-7	breast:
10	chr14:105555507..105557532-chr14:105644874..105649259,4	MCF-7	breast:
11	chr14:105556806..105557482-chr14:105648408..105649374,2	K562	blood:
12	chr14:105556904..105557457-chr14:105630667..105631594,2	MCF-7	breast:
13	chr14:105556047..105558699-chr14:105620485..105622825,2	K562	blood:
14	chr14:105556509..105557265-chr14:105631240..105632200,2	MCF-7	breast:
15	chr14:105556860..105558487-chr14:105603973..105605818,2	K562	blood:
16	chr14:105556465..105557553-chr14:105654009..105655084,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257556	TF binding region
ENSG00000213228	Chromatin interaction
ENSG00000257622	Chromatin interaction
ENSG00000183828	Chromatin interaction
ENSG00000184916	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12147075	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12884077	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28450433	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34283552	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4983577	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4983579	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4983583	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
4	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv902421	chr14:105410183-105574843	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
6	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
7	nsv1052190	chr14:105423761-105722653	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
8	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
9	nsv1042303	chr14:105435649-105633544	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
10	nsv456458	chr14:105435649-105690092	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
11	nsv566150	chr14:105435649-105690092	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
12	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
13	nsv456459	chr14:105459140-105617891	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
14	nsv566152	chr14:105459140-105617891	Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
15	nsv902425	chr14:105463936-105690092	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
16	nsv9175	chr14:105496509-105688941	Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
17	nsv902427	chr14:105508577-105585347	Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
18	esv2758369	chr14:105513346-105803170	Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
19	esv2760014	chr14:105513346-105803170	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105551600-105559000	Enhancers	Placenta	Placenta
2	chr14:105554000-105557800	Enhancers	HMEC	breast
3	chr14:105554000-105559000	Enhancers	Gastric	stomach
4	chr14:105554200-105559000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr14:105554200-105559000	Enhancers	Pancreas	Pancrea
6	chr14:105554400-105557600	Enhancers	NHLF	lung
7	chr14:105554600-105557400	Weak transcription	Aorta	Aorta
8	chr14:105554600-105558400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr14:105554600-105558600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr14:105554600-105558800	Weak transcription	K562	blood
11	chr14:105554600-105559200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr14:105554800-105557800	Weak transcription	Right Atrium	heart
13	chr14:105554800-105559200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr14:105555000-105557200	Weak transcription	HUVEC	blood vessel
15	chr14:105555200-105557200	Weak transcription	HSMMtube	muscle
16	chr14:105555400-105557800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:105555400-105557800	Weak transcription	NHDF-Ad	bronchial
18	chr14:105555400-105559200	Weak transcription	Ovary	ovary
19	chr14:105555600-105557200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr14:105555600-105557200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr14:105555600-105557200	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr14:105555600-105557200	Weak transcription	NH-A	brain
23	chr14:105555600-105557800	Enhancers	Colonic Mucosa	Colon
24	chr14:105555600-105558000	Flanking Active TSS	A549	lung
25	chr14:105555600-105558400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr14:105555600-105559000	Enhancers	Fetal Muscle Leg	muscle
27	chr14:105555800-105558600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr14:105555800-105559000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr14:105556000-105559000	Enhancers	Placenta Amnion	Placenta Amnion
30	chr14:105556200-105557600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr14:105556400-105557400	Enhancers	Primary T cells fromperipheralblood	blood
32	chr14:105556400-105557400	Enhancers	Hela-S3	cervix
33	chr14:105556400-105558200	Enhancers	Muscle Satellite Cultured Cells	--
34	chr14:105556400-105558400	Enhancers	Fetal Intestine Large	intestine
35	chr14:105556400-105559200	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr14:105556400-105559600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr14:105556400-105559800	Enhancers	Spleen	Spleen
38	chr14:105556600-105557200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr14:105556600-105557200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr14:105556600-105557200	Genic enhancers	Fetal Intestine Small	intestine
41	chr14:105556600-105557400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr14:105556600-105557400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr14:105556600-105557400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr14:105556600-105557400	Enhancers	Duodenum Mucosa	Duodenum
45	chr14:105556600-105557600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr14:105556600-105557600	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr14:105556600-105557600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr14:105556600-105557600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr14:105556600-105558200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr14:105556600-105558600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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