Variant report

Variant	rs10873549
Chromosome Location	chr14:105126319-105126320
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:40)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:40 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr14:105125741-105127385	GM12892	blood:	n/a	n/a
2	POLR2A	chr14:105126210-105127344	GM15510	blood:	n/a	n/a
3	SP1	chr14:105126266-105126783	GM12878	blood:	n/a	chr14:105126303-105126312 chr14:105126303-105126313 chr14:105126304-105126313 chr14:105126303-105126312
4	TCF12	chr14:105126304-105126816	GM12878	blood:	n/a	chr14:105126630-105126640
5	PAX5	chr14:105126282-105126765	GM12892	blood:	n/a	n/a
6	POLR2A	chr14:105126258-105126831	GM12892	blood:	n/a	n/a
7	POLR2A	chr14:105126314-105127283	GM19193	blood:	n/a	n/a
8	BCLAF1	chr14:105126267-105126825	GM12878	blood:	n/a	chr14:105126660-105126669
9	POLR2A	chr14:105126292-105127354	GM10847	blood:	n/a	n/a
10	POLR2A	chr14:105126299-105127350	GM18951	blood:	n/a	n/a
11	EBF1	chr14:105126218-105126813	GM12878	blood:	n/a	n/a
12	NFIC	chr14:105126280-105127436	GM12878	blood:	n/a	n/a
13	POLR2A	chr14:105126276-105126716	GM12891	blood:	n/a	n/a
14	MAX	chr14:105126316-105126746	GM12878	blood:	n/a	chr14:105126563-105126572
15	ZNF143	chr14:105126183-105127325	GM12878	blood:	n/a	chr14:105127194-105127212
16	TCF3	chr14:105126151-105126892	GM12878	blood:	n/a	chr14:105126586-105126600
17	NFIC	chr14:105126259-105126858	GM12878	blood:	n/a	n/a
18	RUNX3	chr14:105125982-105126847	GM12878	blood:	n/a	n/a
19	FOXM1	chr14:105126308-105126753	GM12878	blood:	n/a	n/a
20	EP300	chr14:105126263-105126765	GM12878	blood:	n/a	chr14:105126531-105126547 chr14:105126619-105126628
21	POLR2A	chr14:105125904-105127371	GM12892	blood:	n/a	n/a
22	STAT5A	chr14:105126306-105127411	GM12878	blood:	n/a	chr14:105126517-105126525
23	PAX5	chr14:105126223-105127443	GM12878	blood:	n/a	chr14:105127153-105127162 chr14:105127156-105127165
24	YY1	chr14:105126310-105126548	GM12878	blood:	n/a	n/a
25	MTA3	chr14:105125786-105127384	GM12878	blood:	n/a	n/a
26	POLR2A	chr14:105126152-105126790	GM12878	blood:	n/a	n/a
27	ELF1	chr14:105126243-105127384	GM12878	blood:	n/a	chr14:105126619-105126630
28	CHD2	chr14:105126288-105127348	GM12878	blood:	n/a	n/a
29	POLR2A	chr14:105126304-105127731	GM12891	blood:	n/a	n/a
30	MEF2C	chr14:105126192-105126794	GM12878	blood:	n/a	chr14:105126462-105126477
31	RUNX3	chr14:105126284-105126844	GM12878	blood:	n/a	n/a
32	EP300	chr14:105126185-105127373	GM12878	blood:	n/a	chr14:105127198-105127214 chr14:105127153-105127167 chr14:105126531-105126547 chr14:105126619-105126628
33	POLR2A	chr14:105126187-105126569	GM12892	blood:	n/a	n/a
34	ATF2	chr14:105126283-105126793	GM12878	blood:	n/a	n/a
35	POLR2A	chr14:105126313-105126710	GM12878	blood:	n/a	n/a
36	MEF2A	chr14:105126137-105126748	GM12878	blood:	n/a	n/a
37	FOXM1	chr14:105126282-105126824	GM12878	blood:	n/a	n/a
38	POLR2A	chr14:105125341-105127703	GM19099	blood:	n/a	n/a
39	NFATC1	chr14:105126286-105126741	GM12878	blood:	n/a	n/a
40	ELF1	chr14:105126288-105126787	GM12878	blood:	n/a	chr14:105126619-105126630

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105126275-105126325	HL-60	blood:	n/a
2	chr14:105126275-105126325	HCM	heart:	n/a
3	chr14:105126275-105126325	HUVEC	blood vessel:	n/a
4	chr14:105126275-105126325	GM12892	blood:	n/a
5	chr14:105126275-105126325	SK-N-MC	brain:	n/a
6	chr14:105126275-105126325	HNPCEpiC	eye:	n/a
7	chr14:105126275-105126325	T-47D	breast:	n/a
8	chr14:105126275-105126325	AoSMC	blood vessel:	n/a
9	chr14:105126275-105126325	AG09319	gingival:	n/a
10	chr14:105126275-105126325	PrEC	prostate:	n/a
11	chr14:105126275-105126325	SAEC	small airway:	n/a
12	chr14:105126275-105126325	GM12878	blood:	n/a
13	chr14:105126275-105126325	HepG2	liver:	n/a
14	chr14:105126275-105126325	H1-hESC	embryonic stem cell:	embryo
15	chr14:105126275-105126325	AG09309	skin:	n/a
16	chr14:105126275-105126325	Hela-S3	cervix:	n/a
17	chr14:105126275-105126325	ProgFib	skin:	n/a
18	chr14:105126275-105126325	HCPEpiC	choroid plexus:	n/a
19	chr14:105126275-105126325	HMEC	breast:	n/a
20	chr14:105126275-105126325	AG04449	skin:	fetal
21	chr14:105126275-105126325	A549	lung:	n/a
22	chr14:105126275-105126325	NH-A	brain:	n/a
23	chr14:105126275-105126325	SK-N-SH_RA	brain:	n/a
24	chr14:105126275-105126325	RPTEC	kidney:	n/a
25	chr14:105126275-105126325	MCF-7	breast:	n/a
26	chr14:105126275-105126325	PANC-1	pancreas:	n/a
27	chr14:105126275-105126325	HIPEpiC	eye:	n/a
28	chr14:105126275-105126325	Caco-2	colon:	n/a
29	chr14:105126275-105126325	ECC-1	luminal epithelium:	n/a
30	chr14:105126275-105126325	NHBE	bronchial:	n/a
31	chr14:105126275-105126325	SKMC	muscle:	n/a
32	chr14:105126275-105126325	HAEpiC	amniotic membrane:	n/a
33	chr14:105126275-105126325	IMR90	lung:	fetal
34	chr14:105126275-105126325	HEEpiC	esophagus:	n/a
35	chr14:105126275-105126325	LNCaP	prostate:	n/a
36	chr14:105126275-105126325	AG10803	skin:	n/a
37	chr14:105126275-105126325	NHDF-neo	bronchial:	n/a
38	chr14:105126275-105126325	SK-N-SH	brain:	n/a
39	chr14:105126275-105126325	HRPEpiC	eye:	n/a
40	chr14:105126275-105126325	HRE	kidney:	n/a
41	chr14:105126275-105126325	GM19239	blood:	n/a
42	chr14:105126275-105126325	HCF	heart:	n/a
43	chr14:105126275-105126325	GM06990	blood:	n/a
44	chr14:105126275-105126325	GM12891	blood:	n/a
45	chr14:105126275-105126325	HPAEpiC	pulmonary alveolar:	n/a
46	chr14:105126275-105126325	BE2_C	brain:	n/a
47	chr14:105126275-105126325	Jurkat	blood:	n/a
48	chr14:105126275-105126325	BJ	skin:	n/a
49	chr14:105126275-105126325	HEK293	kidney:	embryo
50	chr14:105126275-105126325	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:105124725..105126951-chr14:105154633..105156683,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000258736	TF binding region
ENSG00000258736	CpG island
ENSG00000203485	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12431388	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12433394	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12434207	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12436070	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12436101	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12436635	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28435446	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4371093	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4983377	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4983378	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4983518	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4983524	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4983525	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4983526	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs55639933	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57054585	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57515560	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs59699979	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs59804769	0.82[ASN][1000 genomes]
rs59950617	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs72713869	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72713877	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72713881	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530812	chr14:104775571-105364883	Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription 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 miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1051647	chr14:104983302-105153720	Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
3	nsv542223	chr14:104983302-105153720	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
4	esv1816766	chr14:105007585-105126354	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv902372	chr14:105011436-105200377	Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
6	nsv456445	chr14:105023512-105170003	Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
7	nsv566047	chr14:105023512-105170003	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
8	nsv1053591	chr14:105024558-105475931	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
9	nsv542224	chr14:105024558-105475931	Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
10	nsv902375	chr14:105045524-105139894	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	esv2830002	chr14:105078251-105348552	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
12	nsv902378	chr14:105086475-105200377	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
13	nsv902379	chr14:105086475-105274093	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
14	nsv902380	chr14:105092479-105166002	Genic enhancers Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
15	nsv902381	chr14:105092479-105168414	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
16	nsv902382	chr14:105092479-105185666	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
17	nsv902383	chr14:105092479-105200377	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
18	nsv902384	chr14:105092479-105208567	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
19	nsv902385	chr14:105092479-105215351	Enhancers Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
20	nsv902386	chr14:105092479-105233095	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
21	nsv902387	chr14:105092479-105274093	Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS 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
22	nsv902388	chr14:105092479-105311249	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
23	nsv902389	chr14:105092479-105366499	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
24	nsv902390	chr14:105100021-105185666	Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
25	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
26	nsv902391	chr14:105105769-105185666	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
27	nsv902392	chr14:105105769-105274093	Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats 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	59 gene(s)	inside rSNPs	diseases
28	nsv902393	chr14:105116232-105200377	Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
29	nsv902394	chr14:105116232-105274093	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
30	nsv902395	chr14:105119897-105215351	Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
31	nsv902396	chr14:105119897-105274093	Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105116800-105131600	Weak transcription	Right Atrium	heart
2	chr14:105121800-105126400	Enhancers	Primary B cells from cord blood	blood
3	chr14:105121800-105126400	Enhancers	Fetal Thymus	thymus
4	chr14:105121800-105127400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr14:105122200-105132800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr14:105122800-105127200	Enhancers	Thymus	Thymus
7	chr14:105122800-105127600	Enhancers	Primary T cells from cord blood	blood
8	chr14:105122800-105127800	Enhancers	Primary hematopoietic stem cells	blood
9	chr14:105123000-105127200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr14:105123400-105127400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr14:105123800-105126400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr14:105123800-105131000	Weak transcription	Brain Hippocampus Middle	brain
13	chr14:105124400-105128000	Flanking Active TSS	GM12878-XiMat	blood
14	chr14:105124600-105127400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr14:105124800-105127000	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr14:105124800-105127200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:105125200-105126600	Weak transcription	HepG2	liver
18	chr14:105125200-105127400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
19	chr14:105125400-105127400	Enhancers	Fetal Muscle Leg	muscle
20	chr14:105125600-105127200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr14:105125600-105127200	Enhancers	Placenta	Placenta
22	chr14:105125600-105127400	Bivalent Enhancer	Colonic Mucosa	Colon
23	chr14:105125600-105131200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:105125800-105126400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr14:105125800-105126400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
26	chr14:105125800-105126600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr14:105125800-105126600	Bivalent Enhancer	Fetal Stomach	stomach
28	chr14:105125800-105126800	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr14:105125800-105127400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
30	chr14:105126000-105126600	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr14:105126000-105126600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr14:105126000-105126600	Enhancers	Placenta Amnion	Placenta Amnion
33	chr14:105126000-105126800	Enhancers	H1 Cell Line	embryonic stem cell
34	chr14:105126000-105126800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr14:105126000-105126800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
36	chr14:105126000-105126800	Enhancers	Left Ventricle	heart
37	chr14:105126000-105127000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
38	chr14:105126000-105127000	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
39	chr14:105126000-105127000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
40	chr14:105126000-105127000	Enhancers	Spleen	Spleen
41	chr14:105126000-105127000	Enhancers	HSMM	muscle
42	chr14:105126000-105127200	Flanking Active TSS	Primary B cells from peripheral blood	blood
43	chr14:105126000-105127200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr14:105126000-105127200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
45	chr14:105126000-105127400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
46	chr14:105126000-105128000	Enhancers	HSMMtube	muscle
47	chr14:105126200-105126400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr14:105126200-105126400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr14:105126200-105126600	Weak transcription	Right Ventricle	heart
50	chr14:105126200-105126600	Enhancers	HMEC	breast

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