Variant report

Variant	rs1197672
Chromosome Location	chr15:42103822-42103823
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:277)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr15:42103611-42103863	K562	blood:	n/a	n/a
2	SMC3	chr15:42103559-42104003	Hela-S3	cervix:	n/a	n/a
3	PAX5	chr15:42103627-42103896	GM12878	blood:	n/a	n/a
4	CTCF	chr15:42103590-42103965	SK-N-SH_RA	brain:	n/a	n/a
5	CTCF	chr15:42103720-42103870	HEEpiC	esophagus:	n/a	n/a
6	CTCF	chr15:42103700-42103850	HUVEC	blood vessel:	n/a	n/a
7	CTCF	chr15:42103700-42103850	NB4	blood:	n/a	n/a
8	CTCF	chr15:42103720-42103870	BJ	skin:	n/a	n/a
9	CTCF	chr15:42103680-42103830	AG04450	lung:	n/a	n/a
10	CTCF	chr15:42103680-42103830	A549	lung:	n/a	n/a
11	RCOR1	chr15:42103603-42103884	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr15:42103654-42103931	Gliobla	brain:	n/a	n/a
13	CTCF	chr15:42103700-42103850	GM12872	blood:	n/a	n/a
14	CTCF	chr15:42103680-42103830	HEEpiC	esophagus:	n/a	n/a
15	CTCF	chr15:42103720-42103870	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr15:42103639-42103936	Lung_OC	lung:	n/a	n/a
17	JUND	chr15:42103596-42103942	K562	blood:	n/a	n/a
18	CTCF	chr15:42103511-42104000	HepG2	liver:	n/a	n/a
19	CTCF	chr15:42103550-42103984	T-47D	breast:	n/a	n/a
20	RCOR1	chr15:42103693-42103905	HepG2	liver:	n/a	n/a
21	RAD21	chr15:42103636-42103907	K562	blood:	n/a	n/a
22	MAFK	chr15:42103599-42103894	K562	blood:	n/a	n/a
23	CTCF	chr15:42103720-42103870	K562	blood:	n/a	n/a
24	CTCF	chr15:42103664-42103944	LNCaP	prostate:	n/a	n/a
25	CTCF	chr15:42103666-42103923	Fibrobl	skin:	n/a	n/a
26	CTCF	chr15:42103639-42103952	GM19240	blood:	n/a	n/a
27	RFX5	chr15:42103765-42104090	HepG2	liver:	n/a	n/a
28	CTCF	chr15:42103760-42103910	GM12875	blood:	n/a	n/a
29	RFX5	chr15:42103602-42103952	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr15:42103638-42103935	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr15:42103693-42103927	GM12878	blood:	n/a	n/a
32	USF2	chr15:42103734-42103934	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr15:42103720-42103870	RPTEC	kidney:	n/a	n/a
34	CTCF	chr15:42103740-42103890	GM12872	blood:	n/a	n/a
35	MYBL2	chr15:42103545-42103897	HepG2	liver:	n/a	n/a
36	CTCF	chr15:42103720-42103870	AG10803	skin:	n/a	n/a
37	CTCF	chr15:42103700-42103850	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr15:42103720-42103870	HMEC	breast:	n/a	n/a
39	CTCF	chr15:42103570-42103967	A549	lung:	n/a	n/a
40	RAD21	chr15:42103449-42104098	HepG2	liver:	n/a	n/a
41	CTCF	chr15:42103657-42103944	GM12891	blood:	n/a	n/a
42	ZNF143	chr15:42103613-42103924	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr15:42103584-42103952	IMR90	lung:	n/a	n/a
44	CTCF	chr15:42103700-42103850	HA-sp	spinal cord:	n/a	n/a
45	MAX	chr15:42103649-42103917	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr15:42103548-42104066	K562	blood:	n/a	n/a
47	MXI1	chr15:42103350-42104040	IMR90	lung:	n/a	n/a
48	CHD1	chr15:42103358-42104102	IMR90	lung:	n/a	n/a
49	CTCF	chr15:42103640-42103936	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr15:42103720-42103870	Hela-S3	cervix:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42064231..42067337-chr15:42102963..42104752,21	K562	blood:
2	chr15:41895763..41896358-chr15:42103332..42103836,2	MCF-7	breast:
3	chr15:42066441..42067175-chr15:42103083..42104316,4	MCF-7	breast:
4	chr15:42064618..42065570-chr15:42103319..42104238,3	MCF-7	breast:
5	chr15:41849511..41850438-chr15:42103338..42104256,4	K562	blood:
6	chr15:42063995..42065627-chr15:42103084..42104266,14	MCF-7	breast:
7	chr15:42063685..42066999-chr15:42102378..42105267,3	MCF-7	breast:
8	chr15:41757721..41758661-chr15:42103319..42104236,5	K562	blood:
9	chr15:41988022..41988696-chr15:42103354..42104252,2	K562	blood:
10	chr15:42064035..42067811-chr15:42102222..42105290,4	K562	blood:
11	chr15:42102419..42105107-chr15:42118936..42121739,2	MCF-7	breast:
12	chr15:42066384..42066972-chr15:42103408..42104272,2	MCF-7	breast:

No data

Variant related genes	Relation type
MAPKBP1	TF binding region
ENSG00000092445	Chromatin interaction
ENSG00000260814	Chromatin interaction
ENSG00000137802	Chromatin interaction
ENSG00000243789	Chromatin interaction
ENSG00000168970	Chromatin interaction
ENSG00000250379	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1122884	0.96[CEU][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11630972	0.96[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.87[TSI][hapmap]
rs11631051	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11632519	1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11633160	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634083	0.95[CEU][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634804	0.96[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11636523	0.86[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.82[TSI][hapmap];1.00[ASN][1000 genomes]
rs1197660	0.83[CEU][hapmap]
rs1197667	0.88[CEU][hapmap];1.00[JPT][hapmap];0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1197669	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1197671	0.83[ASW][hapmap];1.00[CEU][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.97[TSI][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1197702	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1197703	0.92[ASW][hapmap];0.96[CEU][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.84[YRI][hapmap];0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1197705	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1197706	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12906666	0.96[CEU][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12917387	0.91[CEU][hapmap];1.00[JPT][hapmap]
rs17677098	0.96[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.89[TSI][hapmap]
rs17677757	0.91[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.87[TSI][hapmap];1.00[ASN][1000 genomes]
rs17678310	0.87[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.82[TSI][hapmap];1.00[ASN][1000 genomes]
rs2178003	0.96[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.89[TSI][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2925339	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.81[TSI][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34621600	1.00[ASN][1000 genomes]
rs35476790	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4923917	0.80[YRI][hapmap]
rs7167078	0.96[CEU][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap]
rs8025614	0.80[YRI][hapmap]
rs8042809	0.87[CEU][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs890497	0.84[AFR][1000 genomes]
rs890503	0.87[TSI][hapmap]
rs9646193	0.96[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.89[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:21 , 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	nsv9243	chr15:42101625-42103990	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	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
20	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
21	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

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs1197672	CAPN3	cis	parietal	SCAN
rs1197672	NDUFAF1	cis	parietal	SCAN
rs1197672	MAPKBP1	cis	cerebellum	SCAN
rs1197672	RPAP1	cis	parietal	SCAN
rs1197672	SNAP23	cis	parietal	SCAN
rs1197672	MAPKBP1	cis	parietal	SCAN
rs1197672	SPTBN5	cis	cerebellum	SCAN

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42070200-42109800	Weak transcription	Fetal Brain Male	brain
2	chr15:42083600-42104600	Weak transcription	Liver	Liver
3	chr15:42083600-42109200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:42083800-42104400	Weak transcription	Colonic Mucosa	Colon
5	chr15:42083800-42105000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr15:42083800-42119400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr15:42089400-42114800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr15:42090000-42109800	Weak transcription	Small Intestine	intestine
9	chr15:42091400-42105400	Weak transcription	HSMMtube	muscle
10	chr15:42092200-42109400	Weak transcription	HepG2	liver
11	chr15:42093200-42104800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr15:42093400-42104000	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr15:42093600-42104200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr15:42093600-42104200	Weak transcription	Dnd41	blood
15	chr15:42093600-42105200	Weak transcription	Brain Germinal Matrix	brain
16	chr15:42094200-42104400	Weak transcription	Fetal Lung	lung
17	chr15:42094200-42104600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr15:42094600-42104400	Weak transcription	Fetal Brain Female	brain
19	chr15:42095200-42104400	Weak transcription	GM12878-XiMat	blood
20	chr15:42097000-42104200	Weak transcription	Aorta	Aorta
21	chr15:42097000-42104800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr15:42097200-42111000	Weak transcription	Fetal Kidney	kidney
23	chr15:42097600-42104200	Weak transcription	Thymus	Thymus
24	chr15:42097600-42104400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr15:42097600-42107800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:42097800-42119600	Weak transcription	Psoas Muscle	Psoas
27	chr15:42098200-42104200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr15:42098200-42118800	Strong transcription	Fetal Stomach	stomach
29	chr15:42098800-42115600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr15:42099000-42104200	Weak transcription	Lung	lung
31	chr15:42099000-42104600	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr15:42099000-42104800	Weak transcription	Pancreas	Pancrea
33	chr15:42099000-42104800	Weak transcription	Rectal Smooth Muscle	rectum
34	chr15:42099000-42110000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr15:42099000-42110000	Weak transcription	Stomach Mucosa	stomach
36	chr15:42099200-42104200	Weak transcription	Right Ventricle	heart
37	chr15:42099200-42104600	Weak transcription	Left Ventricle	heart
38	chr15:42099200-42110000	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr15:42099200-42112000	Weak transcription	A549	lung
40	chr15:42099800-42104200	Weak transcription	Duodenum Mucosa	Duodenum
41	chr15:42100200-42113200	Strong transcription	Fetal Intestine Small	intestine
42	chr15:42100800-42118800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr15:42101000-42104200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr15:42101400-42104200	Enhancers	Primary hematopoietic stem cells	blood
45	chr15:42101600-42104400	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr15:42101800-42104000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr15:42101800-42104000	Weak transcription	Osteobl	bone
48	chr15:42101800-42104200	Weak transcription	NH-A	brain
49	chr15:42101800-42104400	Enhancers	Primary T cells fromperipheralblood	blood
50	chr15:42101800-42104800	Weak transcription	Primary monocytes fromperipheralblood	blood

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