Variant report

Variant	rs10083493
Chromosome Location	chr14:56045411-56045412
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:16)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:16 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:56045300-56045450	HPAF	blood vessel:	n/a	n/a
2	CTCF	chr14:56045340-56045490	BE2_C	brain:	n/a	n/a
3	CTCF	chr14:56045320-56045470	AG04449	skin:	n/a	n/a
4	CTCF	chr14:56045400-56045550	BE2_C	brain:	n/a	n/a
5	POLR2A	chr14:56045364-56046204	SK-N-MC	brain:	n/a	n/a
6	CTCF	chr14:56045300-56045450	AG10803	skin:	n/a	n/a
7	CTCF	chr14:56045280-56045430	NHDF-neo	bronchial:	n/a	n/a
8	CTCF	chr14:56045380-56045530	HPF	lung:	n/a	n/a
9	CTCF	chr14:56045380-56045530	AG09319	gingival:	n/a	n/a
10	CTCF	chr14:56045280-56045430	BJ	skin:	n/a	n/a
11	CTCF	chr14:56045270-56045587	K562	blood:	n/a	n/a
12	MXI1	chr14:56045354-56048230	IMR90	lung:	n/a	n/a
13	CTCF	chr14:56045360-56045510	AG09319	gingival:	n/a	n/a
14	CTCF	chr14:56045385-56045482	Gliobla	brain:	n/a	n/a
15	POLR2A	chr14:56045212-56047473	PANC-1	pancreas:	n/a	n/a
16	CTCF	chr14:56045360-56045510	WERI-Rb-1	eye:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:56044147..56045759-chr14:56045883..56047408,2	MCF-7	breast:
2	chr14:56022620..56026445-chr14:56044953..56047966,3	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBPL2-1	chr14:56045324-56045455	ENSG00000186615
2	lnc-TBPL2-1	chr14:56045324-56045455	ENSG00000186615
3	lnc-TBPL2-1	chr14:56045324-56045455	XLOC_011036
4	lnc-TBPL2-1	chr14:56045324-56045769	XLOC_011036
5	lnc-TBPL2-1	chr14:56045324-56045455	ENSG00000186615.6
6	lnc-TBPL2-1	chr14:56045324-56045455	ENSG00000186615.6

No data

Variant related genes	Relation type
KTN1	TF binding region
ENSG00000126777	Chromatin interaction
ENSG00000186615	Chromatin interaction

Extended variants
information (count: 131 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:122)

rs_ID	r²[population]
rs10083303	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10083353	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10083431	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10083499	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10129890	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10133729	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10133962	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10135124	1.00[YRI][hapmap]
rs10135426	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10135600	0.84[EUR][1000 genomes]
rs10136155	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10137340	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10137364	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10142497	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10142757	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10142869	1.00[YRI][hapmap]
rs10143002	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10145687	0.84[EUR][1000 genomes]
rs10146604	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10147380	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10147431	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10148122	0.80[EUR][1000 genomes]
rs10148188	0.82[AFR][1000 genomes]
rs10148983	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10149408	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10150498	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10151664	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10483643	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10483645	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.88[EUR][1000 genomes]
rs10483646	0.87[CEU][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.84[EUR][1000 genomes]
rs10483648	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[EUR][1000 genomes]
rs10483650	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs11546	0.87[YRI][hapmap];0.80[EUR][1000 genomes]
rs12100753	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];0.88[TSI][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12100949	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12879564	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12879705	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12880362	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12883972	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12886406	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12892022	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs12893061	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12893610	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12893676	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12894368	1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12894613	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13379151	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13379264	0.82[AFR][1000 genomes]
rs13379340	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13379342	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13379343	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13379353	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17253716	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs17253723	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs17253730	0.84[EUR][1000 genomes]
rs17253744	0.84[EUR][1000 genomes]
rs17683614	1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17683626	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17683656	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17683728	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17685078	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.84[EUR][1000 genomes]
rs17685102	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs17745274	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17745459	1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17746033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17746106	0.85[AMR][1000 genomes]
rs17747083	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs17747301	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs17832365	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs17832371	0.84[EUR][1000 genomes]
rs2147114	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2274075	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2296181	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.84[EUR][1000 genomes]
rs28366673	0.82[AFR][1000 genomes]
rs28373835	0.82[AFR][1000 genomes]
rs28380739	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28392709	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28409547	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28478195	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28513551	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28549152	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28581185	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28587929	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28656140	0.94[AFR][1000 genomes]
rs28661008	0.81[EUR][1000 genomes]
rs28681420	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28754619	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28831725	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34136598	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs34330219	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs34446601	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs34719936	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35230683	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35294669	0.88[AMR][1000 genomes]
rs35418987	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35466279	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35536987	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35830444	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3736876	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.84[EUR][1000 genomes]
rs3742570	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3742571	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs45458197	0.84[EUR][1000 genomes]
rs45501402	0.84[EUR][1000 genomes]
rs58569951	0.80[EUR][1000 genomes]
rs58589065	0.80[EUR][1000 genomes]
rs71412688	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs71412689	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs71412690	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs71413577	0.88[AMR][1000 genomes]
rs71413578	0.88[AMR][1000 genomes]
rs7145064	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7150841	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8007065	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8008528	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8009239	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8009608	1.00[YRI][hapmap];0.92[AMR][1000 genomes]
rs8019218	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9323289	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.84[EUR][1000 genomes]
rs9944028	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9972177	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9972178	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9972180	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901958	chr14:55822095-56045411	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv901960	chr14:55853724-56085130	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	nsv901961	chr14:55853724-56101879	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
4	nsv901962	chr14:55862956-56101879	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
5	nsv901963	chr14:55871452-56085130	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv901964	chr14:55871452-56101879	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic 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	29 gene(s)	inside rSNPs	diseases
7	nsv1051564	chr14:55895610-56130788	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	nsv542103	chr14:55895610-56130788	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
9	nsv901965	chr14:55976428-56101879	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10083493	KTN1-AS1	cis	Skin Sun Exposed Lower leg	GTEx
rs10083493	FBXO34	cis	parietal	SCAN
rs10083493	KTN1	cis	multi-tissue	Pritchard

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56024400-56045800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:56025200-56045600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr14:56026200-56045800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:56034200-56046000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:56035600-56045800	Weak transcription	Aorta	Aorta
6	chr14:56037000-56045600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr14:56037400-56045600	Weak transcription	Fetal Kidney	kidney
8	chr14:56037800-56045600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr14:56039000-56045800	Weak transcription	Primary B cells from cord blood	blood
10	chr14:56039600-56045800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr14:56039800-56045600	Weak transcription	Pancreas	Pancrea
12	chr14:56041000-56045600	Weak transcription	Fetal Intestine Small	intestine
13	chr14:56041200-56045800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr14:56041800-56045800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr14:56042000-56045800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:56042000-56045800	Weak transcription	Gastric	stomach
17	chr14:56042000-56045800	Weak transcription	Lung	lung
18	chr14:56042200-56045600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr14:56042400-56045600	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr14:56042400-56045800	Weak transcription	Esophagus	oesophagus
21	chr14:56042800-56045800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr14:56044200-56045600	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr14:56044600-56045600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr14:56044600-56046000	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr14:56044800-56045600	Weak transcription	HUVEC	blood vessel
26	chr14:56045000-56045600	Enhancers	Fetal Brain Male	brain
27	chr14:56045000-56046200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr14:56045200-56045600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr14:56045200-56045600	Enhancers	Primary T cells from cord blood	blood
30	chr14:56045200-56045600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr14:56045200-56045600	Enhancers	Brain Substantia Nigra	brain
32	chr14:56045200-56045600	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr14:56045200-56045600	Enhancers	Dnd41	blood
34	chr14:56045200-56045600	Enhancers	HSMM	muscle
35	chr14:56045200-56045600	Flanking Active TSS	NHLF	lung
36	chr14:56045200-56045800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr14:56045200-56045800	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr14:56045200-56045800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr14:56045200-56045800	Flanking Active TSS	Fetal Heart	heart
40	chr14:56045200-56045800	Flanking Active TSS	Fetal Lung	lung
41	chr14:56045200-56045800	Enhancers	NH-A	brain
42	chr14:56045200-56046000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr14:56045200-56046000	Flanking Active TSS	HSMMtube	muscle
44	chr14:56045200-56048000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr14:56045200-56048200	Active TSS	NHDF-Ad	bronchial
46	chr14:56045200-56048400	Active TSS	Ovary	ovary
47	chr14:56045200-56048400	Active TSS	A549	lung
48	chr14:56045200-56050000	Active TSS	GM12878-XiMat	blood
49	chr14:56045400-56045600	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr14:56045400-56045600	Enhancers	HUES64 Cell Line	embryonic stem cell

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