Variant report

Variant	rs1197688
Chromosome Location	chr15:42115426-42115427
allele	C/T
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	CTCF	chr15:42115400-42115550	Hela-S3	cervix:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
2	CTCF	chr15:42115296-42115722	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
3	RAD21	chr15:42115293-42115738	MCF-7	breast:	n/a	chr15:42115525-42115534 chr15:42115524-42115543
4	CTCF	chr15:42115397-42115652	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
5	MYC	chr15:42115390-42115653	MCF-7	breast:	n/a	n/a
6	CTCF	chr15:42115395-42115658	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
7	CTCF	chr15:42115408-42115640	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
8	CTCF	chr15:42115400-42115550	WERI-Rb-1	eye:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
9	CTCF	chr15:42115328-42115776	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
10	CTCF	chr15:42115400-42115550	HepG2	liver:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
11	CTCF	chr15:42115394-42115643	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
12	CTCF	chr15:42115400-42115550	HBMEC	blood vessel:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
13	CTCF	chr15:42115420-42115570	HMEC	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534
14	RAD21	chr15:42115386-42115755	MCF-7	breast:	n/a	chr15:42115525-42115534 chr15:42115524-42115543
15	CTCF	chr15:42115389-42115645	MCF-7	breast:	n/a	chr15:42115523-42115541 chr15:42115527-42115534

No.	Distal block	Cell Line	Cell type
1	chr15:42115008..42115577-chr15:42196451..42197341,2	MCF-7	breast:
2	chr15:42114988..42115997-chr15:42196197..42197506,6	MCF-7	breast:
3	chr15:42111390..42114154-chr15:42114914..42116415,2	K562	blood:
4	chr15:42114563..42118600-chr15:42118704..42121383,3	K562	blood:

Variant related genes	Relation type
JMJD7-PLA2G4B	TF binding region
PLA2G4B	TF binding region
JMJD7	TF binding region
ENSG00000250379	Chromatin interaction
ENSG00000137802	Chromatin interaction
ENSG00000243789	Chromatin interaction
ENSG00000168970	Chromatin interaction

Extended variants
information (count: 81 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1043627	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1106934	0.93[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11070346	0.82[ASN][1000 genomes]
rs11070349	1.00[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs11547012	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs11630242	0.93[ASN][1000 genomes]
rs11853665	0.81[ASN][1000 genomes]
rs11858843	0.95[CHB][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs1197659	0.93[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.91[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1197662	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs1197668	1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs1197687	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1197689	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.95[TSI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1197690	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1197770	0.82[ASN][1000 genomes]
rs1197773	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1206842	1.00[ASW][hapmap];0.92[CEU][hapmap];0.95[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];0.89[MEX][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1209333	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12439771	0.93[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.81[ASN][1000 genomes]
rs12440605	0.95[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs12591285	0.93[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.94[MEX][hapmap];0.89[TSI][hapmap];0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12595271	0.93[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs12901742	0.93[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs1726915	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1918312	0.93[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.84[ASN][1000 genomes]
rs1918313	0.93[CEU][hapmap];0.90[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.83[ASN][1000 genomes]
rs2077361	0.93[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2077543	1.00[CHB][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs2241523	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs2303517	0.81[CEU][hapmap]
rs2412639	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2412640	0.95[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs2577949	0.93[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs28671571	0.88[ASN][1000 genomes]
rs2925340	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34769385	0.81[ASN][1000 genomes]
rs35033220	0.82[ASN][1000 genomes]
rs35359048	0.86[ASN][1000 genomes]
rs3816533	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.94[TSI][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4923906	0.91[CEU][hapmap];0.81[ASN][1000 genomes]
rs4923907	0.93[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.82[ASN][1000 genomes]
rs4923913	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4923917	1.00[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs4924573	0.92[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs7166139	1.00[CHB][hapmap];0.89[CHD][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs7168489	0.82[ASN][1000 genomes]
rs7173779	0.84[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]
rs7174099	0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs7175346	0.94[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs7177495	0.85[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs883329	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs890504	0.90[ASN][1000 genomes]
rs9806709	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931223	chr15:41989960-42781757	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
2	esv2757597	chr15:42047173-42122617	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	esv2760027	chr15:42047173-42122617	Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv904113	chr15:42050390-42118971	Genic enhancers Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv904114	chr15:42050390-42119900	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv427958	chr15:42051317-42301283	Strong transcription Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS 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	45 gene(s)	inside rSNPs	diseases
7	nsv904115	chr15:42076387-42171483	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
8	nsv904116	chr15:42076387-42229852	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
9	nsv1038393	chr15:42083574-42188035	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers 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	23 gene(s)	inside rSNPs	diseases
10	esv1827003	chr15:42087505-42199076	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer 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	23 gene(s)	inside rSNPs	diseases
11	esv1816120	chr15:42093384-42171578	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
12	nsv1041645	chr15:42095168-42186482	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
13	nsv1051200	chr15:42095168-42188035	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
14	nsv517631	chr15:42096926-42187492	Strong transcription Weak transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
15	nsv1051733	chr15:42098896-42186482	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
16	nsv1036153	chr15:42098896-42188035	Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
17	nsv1035998	chr15:42098896-42434254	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer 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 miRNA	38 gene(s)	inside rSNPs	diseases
18	nsv1048606	chr15:42101694-42192760	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
19	nsv904117	chr15:42103822-42184794	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
20	nsv904118	chr15:42103822-42207905	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
21	nsv904119	chr15:42109975-42142912	Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
22	nsv904120	chr15:42109975-42153085	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
23	nsv904121	chr15:42109975-42162957	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer 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	18 gene(s)	inside rSNPs	diseases
24	nsv904122	chr15:42109975-42166475	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
25	nsv904123	chr15:42109975-42171483	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
26	nsv904124	chr15:42109975-42207905	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
27	nsv9244	chr15:42110712-42208805	Enhancers Genic enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer 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	21 gene(s)	inside rSNPs	diseases
28	esv1008860	chr15:42113556-42117710	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs1197688	NUSAP1	cis	cerebellum	SCAN
rs1197688	MAP1A	cis	parietal	SCAN
rs1197688	VPS18	cis	parietal	SCAN
rs1197688	JMJD7-PLA2G4B	cis	cerebellum	SCAN

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42083800-42119400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:42097800-42119600	Weak transcription	Psoas Muscle	Psoas
3	chr15:42098200-42118800	Strong transcription	Fetal Stomach	stomach
4	chr15:42098800-42115600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr15:42100800-42118800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr15:42101800-42119000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr15:42101800-42119600	Weak transcription	Hela-S3	cervix
8	chr15:42102000-42118600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr15:42103200-42118200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr15:42103600-42116600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr15:42103600-42117400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr15:42103600-42118200	Strong transcription	Placenta	Placenta
13	chr15:42103600-42118200	Strong transcription	NHEK	skin
14	chr15:42103600-42118800	Strong transcription	Spleen	Spleen
15	chr15:42103800-42118000	Strong transcription	Brain Anterior Caudate	brain
16	chr15:42103800-42118800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr15:42103800-42118800	Strong transcription	HMEC	breast
18	chr15:42104000-42117000	Weak transcription	Fetal Heart	heart
19	chr15:42104000-42117200	Strong transcription	Brain Angular Gyrus	brain
20	chr15:42104000-42118200	Strong transcription	Stomach Smooth Muscle	stomach
21	chr15:42104000-42118600	Strong transcription	NHLF	lung
22	chr15:42104000-42118800	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr15:42104000-42119000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr15:42104000-42119000	Strong transcription	Fetal Muscle Leg	muscle
25	chr15:42104200-42117000	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr15:42104200-42117200	Strong transcription	Adipose Nuclei	Adipose
27	chr15:42104200-42117200	Strong transcription	Brain Cingulate Gyrus	brain
28	chr15:42104200-42117800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr15:42104200-42117800	Strong transcription	Fetal Thymus	thymus
30	chr15:42104200-42117800	Strong transcription	Ovary	ovary
31	chr15:42104200-42117800	Strong transcription	Right Ventricle	heart
32	chr15:42104200-42118200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr15:42104200-42118400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr15:42104200-42118600	Strong transcription	Thymus	Thymus
35	chr15:42104200-42118800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr15:42104200-42118800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr15:42104200-42119400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr15:42104200-42119600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr15:42104200-42119600	Weak transcription	K562	blood
40	chr15:42104400-42118600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr15:42104400-42119000	Strong transcription	Fetal Brain Female	brain
42	chr15:42104600-42116200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr15:42104600-42116200	Strong transcription	Left Ventricle	heart
44	chr15:42104600-42116800	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr15:42104600-42117400	Strong transcription	Liver	Liver
46	chr15:42104600-42117600	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr15:42104600-42118200	Strong transcription	Brain Inferior Temporal Lobe	brain
48	chr15:42104600-42118400	Strong transcription	Brain Hippocampus Middle	brain
49	chr15:42104600-42118400	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr15:42104600-42118800	Strong transcription	Primary T cells from cord blood	blood

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