Variant report

Variant	rs8050894
Chromosome Location	chr16:31104509-31104510
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:26)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:26 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr16:31104196-31104857	U87	brain:	n/a	n/a
2	POLR2A	chr16:31104498-31104882	H1-neurons	neurons:	n/a	n/a
3	CTCF	chr16:31104480-31104630	Caco-2	colon:	n/a	n/a
4	BACH1	chr16:31104452-31104717	H1-hESC	embryonic stem cell:	n/a	n/a
5	MAX	chr16:31104508-31104699	K562	blood:	n/a	n/a
6	POLR2A	chr16:31103890-31106642	HepG2	liver:	n/a	n/a
7	RAD21	chr16:31104358-31104679	SK-N-SH_RA	brain:	n/a	n/a
8	IRF1	chr16:31104442-31104910	K562	blood:	n/a	n/a
9	MXI1	chr16:31104381-31105003	HepG2	liver:	n/a	n/a
10	POLR2A	chr16:31104168-31105054	U87	brain:	n/a	n/a
11	MAZ	chr16:31104405-31104919	HepG2	liver:	n/a	n/a
12	SIN3A	chr16:31104436-31105014	H1-hESC	embryonic stem cell:	n/a	n/a
13	SMC3	chr16:31104465-31104616	HepG2	liver:	n/a	n/a
14	MAZ	chr16:31104396-31104754	K562	blood:	n/a	n/a
15	RCOR1	chr16:31104425-31104824	K562	blood:	n/a	n/a
16	CTCF	chr16:31104400-31104550	NB4	blood:	n/a	n/a
17	POLR2A	chr16:31103667-31119079	K562	blood:	n/a	n/a
18	SIN3AK20	chr16:31104337-31104844	SK-N-SH	brain:	n/a	n/a
19	POLR2A	chr16:31104487-31104856	K562	blood:	n/a	n/a
20	POLR2A	chr16:31104425-31104886	HCT-116	colon:	n/a	n/a
21	POLR2A	chr16:31104291-31104583	U87	brain:	n/a	n/a
22	POLR2A	chr16:31103479-31105091	U87	brain:	n/a	n/a
23	MXI1	chr16:31104145-31106481	SK-N-SH	brain:	n/a	n/a
24	ZNF263	chr16:31104339-31104868	HEK293-T-REx	kidney:	n/a	n/a
25	CTCF	chr16:31104381-31104527	K562	blood:	n/a	n/a
26	CTCF	chr16:31104439-31104573	GM12878	blood:	n/a	n/a

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:31043165..31047105-chr16:31102487..31107326,5	MCF-7	breast:
2	chr16:31104440..31108567-chr16:31128079..31131886,5	MCF-7	breast:
3	chr16:31103018..31109714-chr16:31190079..31193155,12	K562	blood:
4	chr16:31104411..31107220-chr16:31127738..31130777,6	K562	blood:
5	chr16:31103889..31108377-chr16:31189247..31192858,8	MCF-7	breast:
6	chr16:30995825..30999208-chr16:31104283..31108641,3	MCF-7	breast:
7	chr16:30993478..30998928-chr16:31103966..31108613,11	MCF-7	breast:
8	chr16:31104000..31106191-chr16:31152891..31155014,2	K562	blood:
9	chr16:30968024..30972662-chr16:31101043..31106214,4	MCF-7	breast:
10	chr16:30958416..30960902-chr16:31103309..31106232,3	MCF-7	breast:
11	chr16:31098290..31102055-chr16:31103024..31106957,5	MCF-7	breast:
12	chr16:31102640..31104934-chr16:31119820..31121678,2	K562	blood:
13	chr16:31103434..31106492-chr16:31118402..31121759,4	K562	blood:
14	chr16:31100062..31102619-chr16:31104236..31105774,2	K562	blood:
15	chr16:31008048..31010924-chr16:31103164..31107386,3	MCF-7	breast:
16	chr16:31076020..31078080-chr16:31104345..31106297,2	MCF-7	breast:
17	chr16:31103018..31108579-chr16:31189579..31192896,9	K562	blood:
18	chr16:31104484..31106009-chr16:31127592..31130114,2	MCF-7	breast:
19	chr16:30968251..30971465-chr16:31104162..31108928,5	MCF-7	breast:

No data

Variant related genes	Relation type
PRSS53	TF binding region
ENSG00000099377	Chromatin interaction
ENSG00000103496	Chromatin interaction
ENSG00000167394	Chromatin interaction
ENSG00000103510	Chromatin interaction
ENSG00000103507	Chromatin interaction
ENSG00000099365	Chromatin interaction
ENSG00000089280	Chromatin interaction
ENSG00000175938	Chromatin interaction
ENSG00000261124	Chromatin interaction
ENSG00000178226	Chromatin interaction
ENSG00000261487	Chromatin interaction
ENSG00000099381	Chromatin interaction
ENSG00000268863	Chromatin interaction
ENSG00000262766	Chromatin interaction
ENSG00000151006	Chromatin interaction
ENSG00000252809	Chromatin interaction

Extended variants
information (count: 143 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:130)

rs_ID	r²[population]
rs1046276	1.00[JPT][hapmap]
rs1060506	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10782001	0.89[JPT][hapmap]
rs10782002	0.89[JPT][hapmap]
rs10871454	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11076	0.88[JPT][hapmap]
rs1108431	0.89[ASN][1000 genomes]
rs11150600	0.89[JPT][hapmap]
rs11150601	0.89[JPT][hapmap]
rs11150604	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11640534	0.89[JPT][hapmap]
rs11640767	0.86[ASN][1000 genomes]
rs11640957	0.86[ASN][1000 genomes]
rs11640961	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs11642003	0.82[ASN][1000 genomes]
rs11642192	0.98[ASN][1000 genomes]
rs11647284	1.00[ASN][1000 genomes]
rs11647442	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11649653	1.00[JPT][hapmap]
rs11862744	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11864806	1.00[ASN][1000 genomes]
rs11864839	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11865038	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11865499	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12102776	0.82[CHB][hapmap]
rs12445650	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12448321	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12597511	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12716981	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12716982	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12924903	1.00[JPT][hapmap]
rs12928852	0.89[JPT][hapmap]
rs12931046	0.89[JPT][hapmap]
rs12934418	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13708	0.89[JPT][hapmap]
rs14235	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1458201	0.89[JPT][hapmap]
rs1458202	0.89[JPT][hapmap]
rs1549293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17839567	0.89[ASN][1000 genomes]
rs17839568	1.00[ASN][1000 genomes]
rs1870293	0.89[JPT][hapmap]
rs1978485	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1978487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2032915	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2054213	0.89[JPT][hapmap]
rs2077633	1.00[YRI][hapmap]
rs2288004	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2303222	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303223	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2305880	0.89[JPT][hapmap]
rs2305884	0.89[JPT][hapmap]
rs2359612	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2855475	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs28725459	0.91[ASN][1000 genomes]
rs28814987	1.00[ASN][1000 genomes]
rs2884738	0.95[ASN][1000 genomes]
rs34649473	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34898535	0.84[EUR][1000 genomes]
rs35351013	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35468353	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs35675346	1.00[JPT][hapmap]
rs35713203	1.00[ASN][1000 genomes]
rs3751855	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4468641	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4527034	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4889525	0.89[JPT][hapmap]
rs4889530	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4889599	0.89[JPT][hapmap]
rs4889603	0.84[CEU][hapmap];0.89[JPT][hapmap]
rs4889604	0.89[JPT][hapmap]
rs4889606	0.96[CEU][hapmap];0.89[JPT][hapmap]
rs4889609	1.00[JPT][hapmap]
rs4889619	0.84[ASN][1000 genomes]
rs4889620	0.95[ASN][1000 genomes]
rs4889623	0.82[CHB][hapmap]
rs55766044	0.95[ASN][1000 genomes]
rs55979739	0.89[ASN][1000 genomes]
rs56284083	0.89[ASN][1000 genomes]
rs56314408	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56813533	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57434408	0.91[ASN][1000 genomes]
rs58726213	0.87[ASN][1000 genomes]
rs59061704	0.86[ASN][1000 genomes]
rs59735493	0.95[ASN][1000 genomes]
rs60996860	0.91[ASN][1000 genomes]
rs61162043	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61320757	0.95[ASN][1000 genomes]
rs6565217	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6950	0.89[JPT][hapmap]
rs7187995	0.93[ASN][1000 genomes]
rs7190802	0.82[CHB][hapmap]
rs7196161	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7196726	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7197717	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7199949	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7200879	1.00[JPT][hapmap]
rs7203999	0.89[JPT][hapmap]
rs7204459	0.89[JPT][hapmap]
rs7206511	0.89[JPT][hapmap]
rs7294	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs729482	1.00[JPT][hapmap]
rs732172	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs732173	0.89[ASN][1000 genomes]
rs73530203	0.98[ASN][1000 genomes]
rs749670	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs749671	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs749767	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7500176	0.89[ASN][1000 genomes]
rs750952	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs8046707	0.89[JPT][hapmap]
rs8047803	1.00[ASN][1000 genomes]
rs8050588	0.89[JPT][hapmap]
rs8056842	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs8060857	0.89[JPT][hapmap]
rs8061047	0.93[ASN][1000 genomes]
rs8062719	0.89[JPT][hapmap]
rs881929	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs889548	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs889555	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs897986	0.89[JPT][hapmap]
rs9923231	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9925964	0.96[CEU][hapmap];0.95[ASN][1000 genomes]
rs9926533	0.96[CEU][hapmap];0.89[JPT][hapmap]
rs9929899	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9934438	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9936329	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs9939417	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9939558	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9972727	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
4	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
5	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
6	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	264 gene(s)	inside rSNPs	diseases
7	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
8	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
9	esv1797877	chr16:30948643-31188432	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
10	nsv833193	chr16:30960796-31133604	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
11	nsv905740	chr16:31066249-31232437	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
12	nsv905741	chr16:31066249-31247924	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
13	nsv905742	chr16:31102321-31247924	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	188 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs8050894	HSD3B7	cis	Whole Blood	GTEx
rs8050894	RP11-196G11.2	cis	Muscle Skeletal	GTEx
rs8050894	KAT8	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31086600-31105200	Weak transcription	Right Atrium	heart
2	chr16:31090000-31105200	Weak transcription	Fetal Kidney	kidney
3	chr16:31092000-31104600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr16:31093000-31104600	Weak transcription	Small Intestine	intestine
5	chr16:31093600-31104800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr16:31093800-31104600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr16:31100800-31104600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr16:31102600-31104600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr16:31102600-31104600	Weak transcription	HSMMtube	muscle
10	chr16:31102800-31104600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr16:31102800-31104600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr16:31102800-31104600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr16:31102800-31104600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr16:31102800-31104600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr16:31102800-31104600	Weak transcription	Primary B cells from cord blood	blood
16	chr16:31102800-31104600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr16:31102800-31104600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr16:31102800-31104600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr16:31102800-31104600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr16:31102800-31104600	Weak transcription	Colonic Mucosa	Colon
21	chr16:31102800-31104600	Weak transcription	Lung	lung
22	chr16:31102800-31104600	Weak transcription	Ovary	ovary
23	chr16:31102800-31104600	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr16:31102800-31104600	Weak transcription	Spleen	Spleen
25	chr16:31102800-31104600	Weak transcription	A549	lung
26	chr16:31102800-31104600	Weak transcription	NHEK	skin
27	chr16:31102800-31104800	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr16:31102800-31104800	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr16:31102800-31105400	Weak transcription	Aorta	Aorta
30	chr16:31103000-31104600	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr16:31103000-31104800	Weak transcription	Fetal Thymus	thymus
32	chr16:31103000-31105000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr16:31103000-31105200	Weak transcription	Fetal Lung	lung
34	chr16:31103000-31105400	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr16:31103400-31104600	Weak transcription	HUVEC	blood vessel
36	chr16:31103600-31104600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr16:31103800-31104600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr16:31103800-31104600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr16:31103800-31104600	Enhancers	Liver	Liver
40	chr16:31103800-31104600	Enhancers	Fetal Brain Male	brain
41	chr16:31103800-31104600	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr16:31103800-31104600	Enhancers	K562	blood
43	chr16:31103800-31104800	Enhancers	Esophagus	oesophagus
44	chr16:31103800-31104800	Enhancers	Pancreas	Pancrea
45	chr16:31103800-31105000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr16:31103800-31105400	Enhancers	Gastric	stomach
47	chr16:31104000-31104600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr16:31104000-31104600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr16:31104000-31104600	Enhancers	Brain Angular Gyrus	brain
50	chr16:31104000-31104600	Enhancers	NH-A	brain

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