Variant report

Variant	rs2494750
Chromosome Location	chr14:105262912-105262913
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	RFX5	chr14:105262905-105262958	HepG2	liver:	n/a	n/a
2	TBP	chr14:105262721-105262991	HepG2	liver:	n/a	n/a
3	HNF4G	chr14:105262675-105263009	HepG2	liver:	n/a	chr14:105262825-105262840 chr14:105262823-105262838 chr14:105262825-105262840 chr14:105262825-105262840 chr14:105262825-105262839
4	CHD2	chr14:105262648-105263144	K562	blood:	n/a	n/a
5	POLR2A	chr14:105262528-105262957	HepG2	liver:	n/a	n/a
6	POLR2A	chr14:105262146-105263193	HepG2	liver:	n/a	n/a
7	POLR2A	chr14:105261858-105263165	HepG2	liver:	n/a	n/a
8	RCOR1	chr14:105262642-105262961	HepG2	liver:	n/a	n/a
9	ZBTB7A	chr14:105262720-105263059	HepG2	liver:	n/a	n/a
10	MAZ	chr14:105262279-105263058	HepG2	liver:	n/a	n/a
11	MAZ	chr14:105262744-105263069	K562	blood:	n/a	n/a
12	MYC	chr14:105262830-105262974	HepG2	liver:	n/a	n/a
13	TBL1XR1	chr14:105262891-105263116	K562	blood:	n/a	n/a
14	EP300	chr14:105262789-105263036	HepG2	liver:	n/a	n/a
15	CTCF	chr14:105262880-105263030	MCF-7	breast:	n/a	n/a
16	POLR2A	chr14:105262644-105263002	HepG2	liver:	n/a	n/a
17	POLR2A	chr14:105260334-105263311	K562	blood:	n/a	n/a
18	ZBTB7A	chr14:105262067-105262974	K562	blood:	n/a	n/a
19	MXI1	chr14:105262633-105263028	HepG2	liver:	n/a	n/a
20	HEY1	chr14:105262553-105263125	HepG2	liver:	n/a	n/a
21	HDAC2	chr14:105262657-105263032	HepG2	liver:	n/a	n/a
22	HNF4A	chr14:105262610-105262958	HepG2	liver:	n/a	chr14:105262825-105262840 chr14:105262825-105262840 chr14:105262825-105262840 chr14:105262825-105262839
23	BHLHE40	chr14:105262625-105263043	HepG2	liver:	n/a	n/a
24	CHD2	chr14:105262807-105263055	HepG2	liver:	n/a	n/a
25	ZBTB7A	chr14:105262674-105263098	HepG2	liver:	n/a	n/a
26	HNF4A	chr14:105262616-105263059	HepG2	liver:	n/a	chr14:105262825-105262840 chr14:105262825-105262840 chr14:105262825-105262840 chr14:105262825-105262839
27	HEY1	chr14:105262822-105263009	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105260251..105263637-chr14:105331262..105334523,4	K562	blood:
2	chr14:105261442..105265036-chr14:105329931..105332556,6	MCF-7	breast:
3	chr14:105260375..105263562-chr14:105329763..105332955,5	MCF-7	breast:
4	chr14:105259095..105269353-chr14:105280422..105289302,26	K562	blood:
5	chr14:105189251..105191715-chr14:105260176..105263336,3	MCF-7	breast:
6	chr14:105145208..105149817-chr14:105259856..105263393,4	MCF-7	breast:
7	chr14:105219293..105222032-chr14:105260458..105263797,3	MCF-7	breast:
8	chr14:105190071..105193724-chr14:105262102..105266779,4	K562	blood:
9	chr14:105188879..105190553-chr14:105260910..105263562,2	MCF-7	breast:

Variant related genes	Relation type
ZBTB42	TF binding region
AKT1	TF binding region
ENSG00000184990	Chromatin interaction
ENSG00000258701	Chromatin interaction
ENSG00000185100	Chromatin interaction
ENSG00000256050	Chromatin interaction
ENSG00000099814	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12878684	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2494741	0.93[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2494742	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2494743	1.00[CEU][hapmap];0.94[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs2494744	1.00[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2494745	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2494746	1.00[CEU][hapmap];0.94[CHB][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs2494749	0.87[ASN][1000 genomes]
rs2494751	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2494752	1.00[CEU][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2498784	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2498785	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2498787	1.00[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2498788	0.88[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2498789	0.88[ASN][1000 genomes]
rs3803300	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4983387	0.94[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs61995965	0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:40 , 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	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	nsv566052	chr14:105126354-105268228	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
14	nsv470677	chr14:105126354-105348552	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
15	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
16	nsv566053	chr14:105139894-105268228	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
17	nsv902397	chr14:105139894-105268228	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
18	nsv517038	chr14:105146579-105311249	Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
19	nsv566057	chr14:105146579-105311249	Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
20	nsv566059	chr14:105148655-105268228	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
21	nsv566060	chr14:105148655-105311249	Flanking Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS 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	66 gene(s)	inside rSNPs	diseases
22	nsv902404	chr14:105148655-105311249	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
23	nsv902405	chr14:105148655-105340643	Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
24	nsv542226	chr14:105153660-105265857	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
25	nsv902407	chr14:105154105-105268228	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
26	nsv902408	chr14:105154105-105274093	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
27	nsv902409	chr14:105154105-105311249	Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
28	nsv566063	chr14:105154105-105312935	Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
29	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
30	nsv902411	chr14:105163532-105268228	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
31	nsv566069	chr14:105185666-105274538	Bivalent/Poised TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
32	nsv902412	chr14:105238701-105361934	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers 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	53 gene(s)	inside rSNPs	diseases
33	nsv566071	chr14:105242831-105274763	Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
34	nsv566072	chr14:105245251-105274712	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
35	esv1836552	chr14:105246686-105348552	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
36	nsv902413	chr14:105246686-105366499	Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
37	nsv902414	chr14:105246989-105274093	Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
38	nsv902415	chr14:105250045-105270554	Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
39	esv3528012	chr14:105260807-105263255	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
40	esv3528013	chr14:105260807-105263255	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105261400-105266000	Weak transcription	Fetal Kidney	kidney
2	chr14:105262200-105263000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
3	chr14:105262200-105263000	Flanking Active TSS	Colonic Mucosa	Colon
4	chr14:105262200-105263000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
5	chr14:105262200-105263000	Flanking Active TSS	Dnd41	blood
6	chr14:105262200-105263200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:105262200-105263200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr14:105262200-105263200	Flanking Active TSS	Stomach Smooth Muscle	stomach
9	chr14:105262200-105263600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr14:105262200-105264400	Enhancers	Fetal Lung	lung
11	chr14:105262400-105263000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr14:105262400-105263000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr14:105262400-105263000	Flanking Active TSS	Duodenum Mucosa	Duodenum
14	chr14:105262400-105263000	Flanking Active TSS	K562	blood
15	chr14:105262400-105263800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr14:105262400-105264000	Weak transcription	NHLF	lung
17	chr14:105262400-105264400	Enhancers	HSMMtube	muscle
18	chr14:105262400-105264600	Enhancers	Lung	lung
19	chr14:105262400-105265000	Enhancers	Fetal Heart	heart
20	chr14:105262400-105266400	Enhancers	Spleen	Spleen
21	chr14:105262600-105263000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
22	chr14:105262600-105263000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
23	chr14:105262600-105263000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr14:105262600-105263000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr14:105262600-105263000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr14:105262600-105263000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr14:105262600-105263000	Flanking Bivalent TSS/Enh	HepG2	liver
28	chr14:105262600-105263200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
29	chr14:105262600-105263200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr14:105262600-105263400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr14:105262600-105263400	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr14:105262600-105263400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr14:105262600-105263400	Weak transcription	Esophagus	oesophagus
34	chr14:105262600-105263400	Bivalent Enhancer	Thymus	Thymus
35	chr14:105262600-105263600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:105262600-105263600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr14:105262600-105263600	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr14:105262600-105263800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr14:105262600-105264000	Enhancers	GM12878-XiMat	blood
40	chr14:105262600-105264200	Enhancers	Left Ventricle	heart
41	chr14:105262600-105264400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr14:105262600-105264600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr14:105262600-105264600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr14:105262600-105264600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr14:105262600-105264600	Bivalent Enhancer	Fetal Thymus	thymus
46	chr14:105262600-105264600	Enhancers	Placenta Amnion	Placenta Amnion
47	chr14:105262600-105264600	Enhancers	Right Ventricle	heart
48	chr14:105262600-105264800	Bivalent Enhancer	Fetal Stomach	stomach
49	chr14:105262600-105265000	Enhancers	Primary hematopoietic stem cells	blood
50	chr14:105262600-105265000	Enhancers	Pancreas	Pancrea

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