Variant report

Variant	rs12627754
Chromosome Location	chr22:20305357-20305358
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:164)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:164 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr22:20305240-20305390	AG09319	gingival:	n/a	n/a
2	CTCF	chr22:20305117-20305493	IMR90	lung:	n/a	n/a
3	MYC	chr22:20305118-20305528	MCF10A-Er-Src	breast:	n/a	chr22:20305332-20305341
4	ZNF143	chr22:20305148-20305363	GM12878	blood:	n/a	n/a
5	JUN	chr22:20305131-20305525	K562	blood:	n/a	n/a
6	CTCF	chr22:20305260-20305410	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr22:20305240-20305390	GM12865	blood:	n/a	n/a
8	CTCF	chr22:20305140-20305392	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr22:20305152-20305407	HepG2	liver:	n/a	n/a
10	CTCF	chr22:20305260-20305410	GM06990	blood:	n/a	n/a
11	CTCF	chr22:20305260-20305410	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr22:20305240-20305390	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr22:20305260-20305410	HEK293	kidney:	n/a	n/a
14	CTCF	chr22:20305280-20305430	AG04450	lung:	n/a	n/a
15	CTCF	chr22:20305167-20305362	MCF-7	breast:	n/a	n/a
16	CTCF	chr22:20305164-20305382	MCF-7	breast:	n/a	n/a
17	CTCF	chr22:20305150-20305364	Fibrobl	skin:	n/a	n/a
18	CTCF	chr22:20305280-20305430	MCF-7	breast:	n/a	n/a
19	CTCF	chr22:20305260-20305410	HRPEpiC	eye:	n/a	n/a
20	POLR2A	chr22:20304942-20305510	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr22:20305280-20305430	GM12869	blood:	n/a	n/a
22	CTCF	chr22:20305086-20305434	GM12878	blood:	n/a	n/a
23	CTCF	chr22:20305240-20305390	BJ	skin:	n/a	n/a
24	CTCF	chr22:20304880-20305501	K562	blood:	n/a	n/a
25	CTCF	chr22:20305280-20305430	GM12872	blood:	n/a	n/a
26	MYC	chr22:20305187-20305367	MCF10A-Er-Src	breast:	n/a	chr22:20305332-20305341
27	CTCF	chr22:20304807-20305572	K562	blood:	n/a	n/a
28	RAD21	chr22:20305122-20305402	K562	blood:	n/a	n/a
29	CTCF	chr22:20305220-20305370	HepG2	liver:	n/a	n/a
30	MYC	chr22:20305170-20305369	K562	blood:	n/a	chr22:20305332-20305341
31	CTCF	chr22:20305260-20305410	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr22:20305280-20305430	NHLF	lung:	n/a	n/a
33	ZNF143	chr22:20305127-20305379	K562	blood:	n/a	n/a
34	CTCF	chr22:20305280-20305430	HAc	cerebellar:	n/a	n/a
35	CTCF	chr22:20305167-20305375	MCF-7	breast:	n/a	n/a
36	CTCF	chr22:20305240-20305390	AoAF	blood vessel:	n/a	n/a
37	CTCFL	chr22:20305242-20305401	K562	blood:	n/a	n/a
38	CTCF	chr22:20305159-20305399	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr22:20305260-20305410	HMEC	breast:	n/a	n/a
40	CTCF	chr22:20305148-20305401	GM19239	blood:	n/a	n/a
41	CTCF	chr22:20305260-20305410	AG09319	gingival:	n/a	n/a
42	CTCF	chr22:20305240-20305390	GM12870	blood:	n/a	n/a
43	JUND	chr22:20305142-20305359	K562	blood:	n/a	n/a
44	CTCF	chr22:20305260-20305410	GM12864	blood:	n/a	n/a
45	RAD21	chr22:20305120-20305392	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr22:20305179-20305444	Lung_OC	lung:	n/a	n/a
47	CTCF	chr22:20305280-20305430	BE2_C	brain:	n/a	n/a
48	MYC	chr22:20305143-20305421	K562	blood:	n/a	chr22:20305332-20305341
49	POLR2A	chr22:20303063-20305836	K562	blood:	n/a	n/a
50	CTCF	chr22:20305139-20305389	ProgFib	skin:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:20256486..20259249-chr22:20304695..20307544,2	K562	blood:
2	chr22:20111134..20113981-chr22:20304973..20307927,2	K562	blood:
3	chr22:20305008..20309233-chr22:20745056..20749818,6	K562	blood:
4	chr22:18895893..18896516-chr22:20304854..20305408,2	MCF-7	breast:
5	chr22:20304415..20312117-chr22:20747096..20751443,9	MCF-7	breast:
6	chr22:20304862..20305860-chr22:20772145..20772996,2	K562	blood:
7	chr22:20284063..20288249-chr22:20303567..20308986,5	K562	blood:
8	chr22:20144264..20145182-chr22:20304502..20305927,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000273139	TF binding region
ENSG00000183628	Chromatin interaction
ENSG00000264346	Chromatin interaction
ENSG00000099901	Chromatin interaction
ENSG00000185252	Chromatin interaction
ENSG00000040608	Chromatin interaction
ENSG00000161132	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1056804	1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1210829	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs5993952	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6518604	1.00[CEU][hapmap]
rs901790	0.82[ASN][1000 genomes]
rs9618779	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1792516	chr22:19578312-20314496	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	195 gene(s)	inside rSNPs	diseases
2	esv1818018	chr22:19674772-20313261	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	193 gene(s)	inside rSNPs	diseases
3	nsv828938	chr22:19678592-20311988	Strong transcription Genic enhancers Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	192 gene(s)	inside rSNPs	diseases
4	nsv828939	chr22:19683555-20311988	Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers 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 miRNA target site	192 gene(s)	inside rSNPs	diseases
5	esv1826873	chr22:19726464-20313261	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
6	nsv588237	chr22:19749525-20306993	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
7	nsv588239	chr22:19907099-20309393	Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
8	nsv471183	chr22:20006040-20306993	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers 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	148 gene(s)	inside rSNPs	diseases
9	esv2758536	chr22:20026493-20309447	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
10	esv2758825	chr22:20026493-20309447	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv828950	chr22:20057967-20311988	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
12	esv1793574	chr22:20075870-20728868	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv914332	chr22:20082961-20339310	Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
14	nsv914337	chr22:20087539-20330895	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
15	esv1832132	chr22:20089802-20728868	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
16	nsv1061349	chr22:20091394-20734304	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
17	esv1804395	chr22:20093565-20485443	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
18	esv1850291	chr22:20093565-20666528	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
19	esv1824760	chr22:20093565-20728868	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
20	nsv1062789	chr22:20100465-20749579	Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
21	nsv828951	chr22:20109578-20310046	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
22	nsv869949	chr22:20126918-20719112	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
23	nsv914360	chr22:20165632-20339310	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
24	nsv914361	chr22:20181136-20313299	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
25	nsv914366	chr22:20189077-20306993	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
26	nsv914375	chr22:20210055-20306993	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
27	nsv519102	chr22:20286099-20306993	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
28	nsv588253	chr22:20287286-20344527	Flanking Active TSS Active TSS Enhancers Weak transcription Genic 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	23 gene(s)	inside rSNPs	diseases
29	nsv979635	chr22:20295282-20321676	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
30	esv1847376	chr22:20295573-20485443	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
31	esv1812390	chr22:20301036-20367573	Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:20287600-20306200	Weak transcription	Gastric	stomach
2	chr22:20292800-20306200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr22:20293600-20305800	Weak transcription	Primary B cells from peripheral blood	blood
4	chr22:20294000-20305600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr22:20295400-20306800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr22:20297000-20305800	Weak transcription	HSMMtube	muscle
7	chr22:20297000-20306200	Weak transcription	Placenta	Placenta
8	chr22:20297200-20305800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr22:20297600-20306200	Weak transcription	Colonic Mucosa	Colon
10	chr22:20297800-20306800	Weak transcription	Aorta	Aorta
11	chr22:20298400-20306800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr22:20299200-20306600	Enhancers	Liver	Liver
13	chr22:20300400-20305800	Weak transcription	Colon Smooth Muscle	Colon
14	chr22:20300800-20306600	Weak transcription	Right Atrium	heart
15	chr22:20301000-20306200	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr22:20302000-20305800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr22:20302600-20305400	Weak transcription	HepG2	liver
18	chr22:20302800-20305800	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr22:20302800-20306200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr22:20303000-20305800	Weak transcription	Ovary	ovary
21	chr22:20303400-20306200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr22:20303400-20306600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr22:20303600-20306600	Weak transcription	Thymus	Thymus
24	chr22:20303800-20306600	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr22:20304000-20306200	Enhancers	Brain Angular Gyrus	brain
26	chr22:20304000-20306200	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr22:20304000-20306600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr22:20304000-20306600	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr22:20304200-20305400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr22:20304200-20305600	Enhancers	Placenta Amnion	Placenta Amnion
31	chr22:20304200-20305800	Enhancers	Dnd41	blood
32	chr22:20304200-20306200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr22:20304200-20306200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr22:20304200-20306400	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr22:20304200-20306400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr22:20304200-20306400	Enhancers	Fetal Heart	heart
37	chr22:20304200-20306400	Enhancers	Stomach Smooth Muscle	stomach
38	chr22:20304200-20306600	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr22:20304200-20306600	Enhancers	Fetal Muscle Leg	muscle
40	chr22:20304200-20306600	Enhancers	Left Ventricle	heart
41	chr22:20304200-20306800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr22:20304400-20305400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr22:20304400-20306200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr22:20304400-20306200	Enhancers	Fetal Brain Male	brain
45	chr22:20304400-20306400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr22:20304400-20306400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr22:20304400-20306600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr22:20304400-20306600	Enhancers	Primary T cells fromperipheralblood	blood
49	chr22:20304400-20306600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr22:20304400-20306600	Enhancers	Adipose Nuclei	Adipose

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