Variant report

Variant	rs1531140
Chromosome Location	chr15:42125234-42125235
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:34)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:34 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr15:42125043-42125353	GM12878	blood:	n/a	n/a
2	STAT3	chr15:42125152-42125359	MCF10A-Er-Src	breast:	n/a	n/a
3	POLR2A	chr15:42124571-42125549	ECC-1	luminal epithelium:	n/a	n/a
4	POLR2A	chr15:42124975-42125520	ECC-1	luminal epithelium:	n/a	n/a
5	CEBPB	chr15:42124968-42125593	ECC-1	luminal epithelium:	n/a	n/a
6	TCF12	chr15:42124861-42125592	ECC-1	luminal epithelium:	n/a	chr15:42125129-42125139
7	EP300	chr15:42125028-42125588	ECC-1	luminal epithelium:	n/a	n/a
8	YY1	chr15:42125100-42125498	ECC-1	luminal epithelium:	n/a	n/a
9	TEAD4	chr15:42124900-42125722	ECC-1	luminal epithelium:	n/a	n/a
10	FOS	chr15:42125095-42125487	MCF10A-Er-Src	breast:	n/a	n/a
11	TEAD4	chr15:42124938-42125614	ECC-1	luminal epithelium:	n/a	n/a
12	MAX	chr15:42124765-42125628	ECC-1	luminal epithelium:	n/a	n/a
13	NFIC	chr15:42124871-42125611	ECC-1	luminal epithelium:	n/a	n/a
14	MYC	chr15:42124988-42125612	MCF10A-Er-Src	breast:	n/a	n/a
15	CEBPB	chr15:42124921-42125585	ECC-1	luminal epithelium:	n/a	n/a
16	RAD21	chr15:42125056-42125493	ECC-1	luminal epithelium:	n/a	n/a
17	MYC	chr15:42125012-42125597	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr15:42125076-42125475	MCF10A-Er-Src	breast:	n/a	n/a
19	PAX5	chr15:42125069-42125354	GM12878	blood:	n/a	n/a
20	FOS	chr15:42125143-42125490	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr15:42125012-42125505	MCF10A-Er-Src	breast:	n/a	n/a
22	USF1	chr15:42124983-42125508	ECC-1	luminal epithelium:	n/a	n/a
23	EP300	chr15:42124790-42125606	ECC-1	luminal epithelium:	n/a	n/a
24	NR3C1	chr15:42124964-42125508	ECC-1	luminal epithelium:	n/a	n/a
25	RAD21	chr15:42124912-42125568	ECC-1	luminal epithelium:	n/a	n/a
26	NFIC	chr15:42124918-42125580	ECC-1	luminal epithelium:	n/a	n/a
27	FOXM1	chr15:42124841-42125626	ECC-1	luminal epithelium:	n/a	n/a
28	YY1	chr15:42125010-42125443	ECC-1	luminal epithelium:	n/a	n/a
29	STAT3	chr15:42125100-42125359	MCF10A-Er-Src	breast:	n/a	n/a
30	TCF12	chr15:42124762-42125768	ECC-1	luminal epithelium:	n/a	chr15:42125129-42125139
31	MAX	chr15:42124754-42125715	ECC-1	luminal epithelium:	n/a	n/a
32	FOXM1	chr15:42124851-42125568	ECC-1	luminal epithelium:	n/a	n/a
33	POLR2A	chr15:42125065-42125591	MCF10A-Er-Src	breast:	n/a	n/a
34	USF1	chr15:42124938-42125582	ECC-1	luminal epithelium:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42122872..42126047-chr15:42126791..42131021,4	K562	blood:
2	chr15:42121774..42125537-chr15:42128092..42132193,4	MCF-7	breast:
3	chr15:42119641..42122495-chr15:42123255..42125312,3	K562	blood:
4	chr15:42119169..42123691-chr15:42124459..42130624,7	MCF-7	breast:

No data

Variant related genes	Relation type
JMJD7	TF binding region
PLA2G4B	TF binding region
JMJD7-PLA2G4B	TF binding region
ENSG00000243708	Chromatin interaction
ENSG00000243789	Chromatin interaction
ENSG00000168970	Chromatin interaction
ENSG00000250379	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1105881	0.89[CEU][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes]
rs1107858	0.92[CEU][hapmap];0.84[JPT][hapmap]
rs11632424	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11634956	0.86[JPT][hapmap]
rs11635067	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11635415	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12440747	0.96[CEU][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12441300	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16971976	0.86[JPT][hapmap]
rs17677199	0.96[CEU][hapmap];0.93[JPT][hapmap]
rs17677991	0.96[CEU][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17678138	0.96[CEU][hapmap];0.93[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17678552	0.96[CEU][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17678767	0.96[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17734856	0.92[CEU][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap]
rs1918310	0.92[CEU][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2241522	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2277535	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2303516	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2303518	0.96[CEU][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2305654	0.92[CEU][hapmap];0.92[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2412641	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2577960	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28373318	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28401754	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28432037	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28451764	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28680296	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28701757	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28754734	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3179542	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3743024	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3959569	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4923910	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4923914	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4923915	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4924570	0.92[JPT][hapmap]
rs4924575	0.96[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4924576	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4924580	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62002090	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62002091	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8025714	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8035855	0.86[JPT][hapmap]
rs890498	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs890505	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9920903	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 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	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	nsv904125	chr15:42119900-42210393	Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1531140	MGA	Cis_1M	lymphoblastoid	RTeQTL
rs1531140	MGA	cis	lesional skin	skin_eQTL

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42121000-42147400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:42121200-42126000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chr15:42121200-42126600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr15:42121200-42130400	Weak transcription	Stomach Mucosa	stomach
5	chr15:42121400-42125400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr15:42121400-42125400	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr15:42121400-42126200	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr15:42121400-42126200	Weak transcription	Ovary	ovary
9	chr15:42121400-42129400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr15:42121400-42130400	Weak transcription	Psoas Muscle	Psoas
11	chr15:42121400-42133800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr15:42121400-42138200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr15:42121400-42138400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr15:42121400-42138400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr15:42121400-42138400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr15:42121400-42138400	Weak transcription	Primary B cells from cord blood	blood
17	chr15:42121400-42147600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr15:42121400-42147600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr15:42121600-42125400	Weak transcription	Fetal Kidney	kidney
20	chr15:42121600-42130200	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr15:42121600-42134000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr15:42121600-42137200	Weak transcription	Osteobl	bone
23	chr15:42121600-42137400	Weak transcription	Small Intestine	intestine
24	chr15:42121600-42138600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr15:42121600-42141400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr15:42121600-42141800	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr15:42121800-42136600	Weak transcription	Brain Substantia Nigra	brain
28	chr15:42121800-42140400	Weak transcription	Hela-S3	cervix
29	chr15:42122000-42133000	Weak transcription	Colon Smooth Muscle	Colon
30	chr15:42122000-42142400	Strong transcription	Fetal Stomach	stomach
31	chr15:42122000-42142600	Strong transcription	Fetal Intestine Small	intestine
32	chr15:42122200-42125400	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
33	chr15:42122200-42126600	Genic enhancers	NHEK	skin
34	chr15:42122200-42128000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr15:42122200-42130200	Weak transcription	Fetal Heart	heart
36	chr15:42122200-42145400	Weak transcription	HepG2	liver
37	chr15:42122400-42125400	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr15:42122400-42126400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr15:42122400-42127400	Weak transcription	Brain Anterior Caudate	brain
40	chr15:42122400-42142600	Weak transcription	Fetal Brain Male	brain
41	chr15:42122800-42125400	Strong transcription	Fetal Brain Female	brain
42	chr15:42122800-42125400	Strong transcription	Stomach Smooth Muscle	stomach
43	chr15:42122800-42125600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr15:42122800-42137200	Weak transcription	NHLF	lung
45	chr15:42123000-42128000	Strong transcription	Fetal Muscle Leg	muscle
46	chr15:42123200-42125600	Genic enhancers	Primary T cells from cord blood	blood
47	chr15:42123200-42126800	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr15:42123200-42130200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr15:42123400-42125600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr15:42123400-42130800	Strong transcription	Primary monocytes fromperipheralblood	blood

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