Variant report

Variant	rs12441932
Chromosome Location	chr15:74909999-74910000
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr15:74906714-74928682	K562	blood:	n/a	n/a
2	POLR2A	chr15:74906801-74910066	Hela-S3	cervix:	n/a	n/a
3	WRNIP1	chr15:74908011-74911036	GM12878	blood:	n/a	n/a
4	POLR2A	chr15:74909865-74910049	K562	blood:	n/a	n/a
5	POLR2A	chr15:74909917-74910228	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:74907146..74910030-chr15:74987199..74990600,3	MCF-7	breast:
2	chr15:74782343..74784266-chr15:74908985..74910885,2	MCF-7	breast:
3	chr15:74908642..74910283-chr15:75091249..75093792,2	MCF-7	breast:
4	chr15:74908350..74910118-chr15:75071323..75073781,2	MCF-7	breast:
5	chr15:74831500..74835189-chr15:74905877..74910530,15	MCF-7	breast:
6	chr15:74909806..74912416-chr15:75659270..75660874,2	MCF-7	breast:
7	chr15:74909966..74912107-chr15:74947107..74949319,2	K562	blood:

No data

Variant related genes	Relation type
CLK3	TF binding region
ENSG00000260919	TF binding region
ENSG00000260103	Chromatin interaction
ENSG00000212279	Chromatin interaction
ENSG00000179361	Chromatin interaction
ENSG00000260274	Chromatin interaction
ENSG00000179151	Chromatin interaction
ENSG00000103653	Chromatin interaction
ENSG00000140400	Chromatin interaction

Extended variants
information (count: 110 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1030889	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs10459601	0.84[TSI][hapmap]
rs10459648	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10851871	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap]
rs10851873	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs11072489	0.81[MKK][hapmap]
rs11072490	0.80[EUR][1000 genomes]
rs11072492	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11072493	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11072494	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11072495	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11072496	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11072497	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11072498	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11072499	0.84[TSI][hapmap]
rs11629749	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11629946	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11854461	0.94[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap]
rs12437519	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12439113	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12442013	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12442097	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12594447	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12909573	0.80[EUR][1000 genomes]
rs1456432	0.87[ASN][1000 genomes]
rs16969247	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs16969393	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs16969612	0.80[EUR][1000 genomes]
rs1821847	0.80[EUR][1000 genomes]
rs1821848	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1866113	0.87[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.80[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap]
rs2061221	0.80[EUR][1000 genomes]
rs2068982	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2198843	1.00[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs2289187	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[TSI][hapmap]
rs2289188	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap]
rs2415241	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2415242	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2415245	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2899826	0.84[TSI][hapmap]
rs3985310	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap]
rs4073149	0.84[TSI][hapmap]
rs4886601	0.89[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4887150	0.94[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap]
rs4887151	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs4887152	0.89[CEU][hapmap];0.90[YRI][hapmap]
rs4887154	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs4887155	0.80[EUR][1000 genomes]
rs4887159	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4887160	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4887162	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4887163	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4887165	0.82[ASN][1000 genomes]
rs4887166	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58473469	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6495104	0.83[TSI][hapmap]
rs6495105	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap]
rs6495106	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs6495112	0.84[TSI][hapmap]
rs6495115	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6495116	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs6495117	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6495118	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6495119	0.84[TSI][hapmap]
rs6495121	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs7161903	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7161990	0.84[TSI][hapmap]
rs7163775	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[TSI][hapmap]
rs7166656	0.80[EUR][1000 genomes]
rs7166701	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[TSI][hapmap]
rs7167655	0.80[EUR][1000 genomes]
rs7171838	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7173006	0.80[EUR][1000 genomes]
rs7176095	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7177407	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7178568	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs74025818	0.94[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7495708	0.81[ASN][1000 genomes]
rs7497036	0.84[TSI][hapmap]
rs7497342	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs750608	0.84[TSI][hapmap]
rs8023479	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs8023865	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8026181	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8026923	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8027066	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8028163	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8028430	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8029116	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8029215	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8036030	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs8037211	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap]
rs8037714	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8040745	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs8041030	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8041807	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8042832	0.80[EUR][1000 genomes]
rs8043082	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9635320	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9672559	0.94[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1809847	chr15:74734500-74948063	Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	esv1812223	chr15:74869438-74948063	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv904379	chr15:74869438-75027880	Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv904380	chr15:74869438-75142761	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer 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	69 gene(s)	inside rSNPs	diseases
5	esv1814078	chr15:74884447-74948063	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	nsv457204	chr15:74885091-74948063	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv569991	chr15:74885091-74948063	Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
8	nsv542434	chr15:74885329-74929552	Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv1047943	chr15:74885329-74940857	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers 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 target site	40 gene(s)	inside rSNPs	diseases
10	nsv817698	chr15:74889163-75019449	Genic enhancers Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74906600-74910000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr15:74908200-74910000	Flanking Active TSS	Primary hematopoietic stem cells	blood
3	chr15:74908400-74910000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
4	chr15:74908600-74910000	Active TSS	Right Atrium	heart
5	chr15:74908600-74910000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
6	chr15:74908800-74910000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr15:74908800-74910200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
8	chr15:74908800-74910600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
9	chr15:74909000-74910000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
10	chr15:74909000-74910000	Enhancers	Spleen	Spleen
11	chr15:74909000-74910200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr15:74909000-74911000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr15:74909000-74927000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr15:74909200-74910000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr15:74909200-74910000	Flanking Active TSS	Fetal Heart	heart
16	chr15:74909200-74910200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr15:74909200-74910400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr15:74909200-74910400	Flanking Active TSS	HMEC	breast
19	chr15:74909400-74910000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr15:74909400-74910000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
21	chr15:74909400-74910000	Weak transcription	Esophagus	oesophagus
22	chr15:74909400-74910000	Enhancers	Fetal Stomach	stomach
23	chr15:74909400-74910000	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr15:74909400-74910000	Transcr. at gene 5' and 3'	K562	blood
25	chr15:74909400-74910000	Flanking Active TSS	NHDF-Ad	bronchial
26	chr15:74909400-74910200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr15:74909400-74910200	Enhancers	Placenta Amnion	Placenta Amnion
28	chr15:74909400-74910400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr15:74909400-74910400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr15:74909400-74910400	Enhancers	Gastric	stomach
31	chr15:74909400-74910600	Enhancers	Primary B cells from peripheral blood	blood
32	chr15:74909400-74910600	Enhancers	Placenta	Placenta
33	chr15:74909400-74910800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr15:74909400-74910800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr15:74909400-74910800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr15:74909400-74910800	Enhancers	Brain Hippocampus Middle	brain
37	chr15:74909400-74910800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr15:74909400-74911200	Enhancers	Stomach Mucosa	stomach
39	chr15:74909400-74911200	Flanking Active TSS	HepG2	liver
40	chr15:74909400-74911400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr15:74909400-74911600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr15:74909400-74911600	Weak transcription	Aorta	Aorta
43	chr15:74909400-74911600	Enhancers	Pancreas	Pancrea
44	chr15:74909400-74911800	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr15:74909600-74910000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:74909600-74910000	Enhancers	Brain Germinal Matrix	brain
47	chr15:74909600-74910000	Enhancers	Fetal Lung	lung
48	chr15:74909600-74910000	Genic enhancers	HSMM	muscle
49	chr15:74909600-74910000	Genic enhancers	NHLF	lung
50	chr15:74909600-74910200	Enhancers	Primary neutrophils fromperipheralblood	blood

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