Variant report

Variant	rs72745053
Chromosome Location	chr15:59159259-59159260
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr15:59159223-59160261	HepG2	liver:	n/a	n/a
2	CTCF	chr15:59159240-59159390	NHEK	skin:	n/a	n/a
3	POLR2A	chr15:59159148-59160400	HepG2	liver:	n/a	n/a
4	RCOR1	chr15:59159245-59159676	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr15:59158040..59159719-chr15:59224699..59227685,2	MCF-7	breast:
2	chr15:59141477..59144121-chr15:59157896..59159549,2	MCF-7	breast:
3	chr15:59150365..59151946-chr15:59158006..59159550,2	K562	blood:
4	chr15:59158497..59160419-chr15:59185793..59188060,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000242747	TF binding region
ENSG00000259353	TF binding region
ENSG00000137776	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs7162694	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34110	chr15:58949991-59381634	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	esv1826703	chr15:59005922-59213678	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	esv1798487	chr15:59027139-59213678	Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv527307	chr15:59103328-60018487	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
5	nsv1035640	chr15:59105360-59190930	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS 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 target site	11 gene(s)	inside rSNPs	diseases
6	nsv904270	chr15:59140329-59238415	Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	nsv977720	chr15:59157444-59165373	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59111800-59159600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:59120000-59169000	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr15:59145000-59166600	Weak transcription	HSMMtube	muscle
4	chr15:59147200-59169000	Weak transcription	K562	blood
5	chr15:59147600-59174600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr15:59148000-59168600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr15:59148000-59169000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr15:59151200-59165400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr15:59154600-59170200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr15:59157200-59168600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr15:59157400-59168800	Weak transcription	Brain Angular Gyrus	brain
12	chr15:59157400-59170400	Weak transcription	Aorta	Aorta
13	chr15:59157600-59159600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr15:59157600-59169000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr15:59157600-59169400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr15:59157600-59169400	Weak transcription	Brain Germinal Matrix	brain
17	chr15:59157600-59170200	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr15:59157600-59170200	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr15:59157600-59170200	Weak transcription	Brain Cingulate Gyrus	brain
20	chr15:59157600-59170200	Weak transcription	Fetal Brain Female	brain
21	chr15:59157800-59159400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr15:59157800-59159400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr15:59157800-59159600	Weak transcription	Spleen	Spleen
24	chr15:59157800-59169000	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr15:59157800-59169400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr15:59157800-59169400	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr15:59157800-59170000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr15:59157800-59170200	Weak transcription	Primary B cells from peripheral blood	blood
29	chr15:59157800-59170200	Weak transcription	Primary T cells from cord blood	blood
30	chr15:59157800-59170400	Weak transcription	Primary B cells from cord blood	blood
31	chr15:59157800-59170400	Weak transcription	Primary hematopoietic stem cells	blood
32	chr15:59157800-59172600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr15:59158000-59162600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr15:59158000-59162600	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr15:59158000-59165400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:59158000-59165600	Weak transcription	Fetal Muscle Leg	muscle
37	chr15:59158000-59167600	Weak transcription	Thymus	Thymus
38	chr15:59158000-59168400	Weak transcription	Gastric	stomach
39	chr15:59158000-59168400	Weak transcription	Stomach Smooth Muscle	stomach
40	chr15:59158000-59168800	Weak transcription	Adipose Nuclei	Adipose
41	chr15:59158000-59169000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr15:59158000-59169000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr15:59158000-59169400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr15:59158000-59170000	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr15:59158000-59170000	Weak transcription	Liver	Liver
46	chr15:59158000-59170000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr15:59158000-59170200	Weak transcription	Left Ventricle	heart
48	chr15:59158000-59170400	Weak transcription	Fetal Lung	lung
49	chr15:59158000-59170400	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr15:59158000-59170600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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