Variant report

Variant	rs2242033
Chromosome Location	chr2:46842410-46842411
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	IRF1	chr2:46842308-46842760	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:46768098..46772914-chr2:46841294..46848059,11	K562	blood:
2	chr2:46768338..46773881-chr2:46842376..46848059,6	K562	blood:
3	chr2:46842180..46843861-chr2:46924432..46926384,2	K562	blood:
4	chr2:46838114..46840779-chr2:46841900..46844194,2	MCF-7	breast:
5	chr2:46770485..46772962-chr2:46842113..46844264,3	MCF-7	breast:

No data

Variant related genes	Relation type
CRIPT	TF binding region
PIGF	TF binding region
ENSG00000171150	Chromatin interaction
ENSG00000119729	Chromatin interaction
ENSG00000250565	Chromatin interaction
ENSG00000151665	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1080871	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11894342	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12104572	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13000706	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13001566	0.82[AMR][1000 genomes]
rs13385693	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1451156	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1531133	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1598517	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1989720	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3087822	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6544906	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6544907	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6739397	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6739468	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6752882	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7598578	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757795	chr2:46532812-46874151	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv2759046	chr2:46532812-46874151	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv1014425	chr2:46670179-47033417	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv535678	chr2:46670179-47033417	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv873996	chr2:46670941-47065227	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv1009735	chr2:46724523-46913152	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv533112	chr2:46800828-46959977	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
8	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS 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 miRNA target site	152 gene(s)	inside rSNPs	diseases
9	nsv873997	chr2:46821640-46984627	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2242033	CRIPT	cis	multi-tissue	Pritchard
rs2242033	CRIPT	cis	Esophagus Muscularis	GTEx
rs2242033	CRIPT	Cis_1M	lymphoblastoid	RTeQTL
rs2242033	CRIPT	cis	Stomach	GTEx

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:46796800-46842800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr2:46802400-46842600	Weak transcription	NHEK	skin
3	chr2:46803400-46842800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr2:46807600-46842600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr2:46807800-46842600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr2:46807800-46842800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:46807800-46842800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr2:46807800-46842800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr2:46807800-46842800	Weak transcription	HSMMtube	muscle
10	chr2:46807800-46843000	Weak transcription	Brain Germinal Matrix	brain
11	chr2:46807800-46843000	Weak transcription	Fetal Stomach	stomach
12	chr2:46807800-46843200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:46808000-46842800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr2:46808600-46842800	Weak transcription	Placenta	Placenta
15	chr2:46809400-46842800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr2:46809600-46842800	Weak transcription	Fetal Thymus	thymus
17	chr2:46810600-46842600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr2:46811600-46842800	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr2:46811800-46843000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr2:46812000-46842600	Weak transcription	Brain Hippocampus Middle	brain
21	chr2:46819600-46842800	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr2:46824200-46842800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr2:46828000-46842800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr2:46828600-46842800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr2:46828600-46842800	Weak transcription	Left Ventricle	heart
26	chr2:46829000-46842800	Weak transcription	Brain Angular Gyrus	brain
27	chr2:46829200-46842600	Weak transcription	Brain Substantia Nigra	brain
28	chr2:46829800-46843200	Weak transcription	Ovary	ovary
29	chr2:46831600-46842800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr2:46833600-46843200	Weak transcription	Colon Smooth Muscle	Colon
31	chr2:46834200-46842600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr2:46834200-46842800	Weak transcription	Liver	Liver
33	chr2:46834600-46842800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr2:46834600-46842800	Weak transcription	Right Ventricle	heart
35	chr2:46835200-46842800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr2:46835400-46842800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr2:46835800-46843000	Weak transcription	Fetal Brain Male	brain
38	chr2:46836600-46842600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr2:46836600-46842800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr2:46836600-46842800	Weak transcription	Stomach Smooth Muscle	stomach
41	chr2:46836800-46842800	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr2:46837200-46842800	Weak transcription	Spleen	Spleen
43	chr2:46837200-46842800	Weak transcription	NH-A	brain
44	chr2:46837400-46842600	Weak transcription	Fetal Lung	lung
45	chr2:46837400-46842800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr2:46838000-46842800	Weak transcription	Psoas Muscle	Psoas
47	chr2:46838200-46842600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:46838200-46842800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr2:46838200-46842800	Weak transcription	Adipose Nuclei	Adipose
50	chr2:46838400-46842600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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