Variant report

Variant	rs35926650
Chromosome Location	chr12:32550835-32550836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:25)
CpG islands
(count:0)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:25 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TEAD4	chr12:32550550-32551025	ECC-1	luminal epithelium:	n/a	n/a
2	E2F6	chr12:32550617-32551188	H1-hESC	embryonic stem cell:	n/a	n/a
3	EP300	chr12:32550528-32551096	ECC-1	luminal epithelium:	n/a	n/a
4	MAX	chr12:32550693-32550988	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr12:32550660-32550847	H1-hESC	embryonic stem cell:	n/a	n/a
6	TEAD4	chr12:32550477-32551151	ECC-1	luminal epithelium:	n/a	n/a
7	EP300	chr12:32550321-32551213	ECC-1	luminal epithelium:	n/a	chr12:32550480-32550494
8	ESR1	chr12:32550576-32550997	ECC-1	luminal epithelium:	n/a	n/a
9	MAX	chr12:32550732-32551004	H1-hESC	embryonic stem cell:	n/a	n/a
10	TCF12	chr12:32550475-32551252	ECC-1	luminal epithelium:	n/a	n/a
11	YY1	chr12:32550530-32551117	ECC-1	luminal epithelium:	n/a	chr12:32550892-32550904
12	YY1	chr12:32550709-32551047	H1-hESC	embryonic stem cell:	n/a	chr12:32550892-32550904
13	MAX	chr12:32550455-32551179	ECC-1	luminal epithelium:	n/a	n/a
14	TCF12	chr12:32550328-32551186	ECC-1	luminal epithelium:	n/a	n/a
15	MAX	chr12:32550538-32551154	ECC-1	luminal epithelium:	n/a	n/a
16	FOXM1	chr12:32550363-32551194	ECC-1	luminal epithelium:	n/a	n/a
17	NFIC	chr12:32550369-32551261	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr12:32550543-32550989	ECC-1	luminal epithelium:	n/a	n/a
19	ESR1	chr12:32550588-32550926	ECC-1	luminal epithelium:	n/a	n/a
20	ESR1	chr12:32550569-32550926	ECC-1	luminal epithelium:	n/a	n/a
21	NFIC	chr12:32550403-32551180	ECC-1	luminal epithelium:	n/a	n/a
22	YY1	chr12:32550605-32551120	ECC-1	luminal epithelium:	n/a	chr12:32550892-32550904
23	YY1	chr12:32550607-32551131	H1-hESC	embryonic stem cell:	n/a	chr12:32550892-32550904
24	E2F6	chr12:32550706-32551023	H1-hESC	embryonic stem cell:	n/a	n/a
25	NR3C1	chr12:32550588-32550986	ECC-1	luminal epithelium:	n/a	n/a

No data

Variant related genes	Relation type
FGD4	TF binding region
ENSG00000207176	TF binding region

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10844195	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11051966	0.90[ASN][1000 genomes]
rs11051967	0.90[ASN][1000 genomes]
rs11051980	0.93[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	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	esv2751096	chr12:32280340-32702784	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv558171	chr12:32287259-32559693	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv469346	chr12:32531220-32587465	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv558188	chr12:32531220-32587465	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1054191	chr12:32534619-32733066	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv541455	chr12:32534619-32733066	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32544200-32551600	Weak transcription	Gastric	stomach
2	chr12:32544200-32551800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr12:32544400-32551800	Weak transcription	Ovary	ovary
4	chr12:32544400-32551800	Weak transcription	HUVEC	blood vessel
5	chr12:32544600-32551200	Weak transcription	Fetal Intestine Large	intestine
6	chr12:32544600-32551600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:32548400-32551600	Weak transcription	A549	lung
8	chr12:32550000-32551200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr12:32550200-32551600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:32550400-32551000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:32550400-32551400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr12:32550400-32551400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr12:32550400-32551400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr12:32550600-32551400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr12:32550600-32551400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr12:32550600-32551400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr12:32550600-32551600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr12:32550600-32551600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:32550600-32551600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:32550600-32551800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr12:32550600-32551800	Enhancers	Brain Cingulate Gyrus	brain
22	chr12:32550800-32551000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr12:32550800-32551200	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr12:32550800-32551400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr12:32550800-32551400	Enhancers	H9 Cell Line	embryonic stem cell
26	chr12:32550800-32551800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr12:32550800-32551800	Enhancers	Pancreas	Pancrea
28	chr12:32550800-32552200	Enhancers	Sigmoid Colon	Sigmoid Colon

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