Variant report

Variant	rs17163384
Chromosome Location	chr1:222835222-222835223
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:222829766-222841488	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:222832045..222836526-chr1:222836686..222840322,4	K562	blood:
2	chr1:222816933..222819100-chr1:222834674..222837406,2	K562	blood:

Variant related genes	Relation type
MIA3	TF binding region
ENSG00000272750	TF binding region
ENSG00000154305	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10495197	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1053316	0.82[MEX][hapmap]
rs11118971	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11485122	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11487815	0.86[ASW][hapmap];1.00[CEU][hapmap];0.88[GIH][hapmap];0.82[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12058171	0.84[MKK][hapmap]
rs17163303	0.82[CEU][hapmap];0.88[GIH][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17163343	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17163373	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17163416	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17163431	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17163441	0.81[LWK][hapmap];0.91[MKK][hapmap];0.87[YRI][hapmap]
rs17530776	0.97[EUR][1000 genomes]
rs17531063	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17531300	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17531468	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3008633	0.82[MEX][hapmap]
rs3008634	0.82[MEX][hapmap]
rs35397194	1.00[ASN][1000 genomes]
rs3748629	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74145506	1.00[ASN][1000 genomes]
rs74145508	1.00[ASN][1000 genomes]
rs74145511	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999185	chr1:222500725-223278032	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv535304	chr1:222500725-223278032	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv873205	chr1:222718718-222923351	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv1012537	chr1:222755091-223512243	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:222818800-222841600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:222819000-222841800	Strong transcription	HUES64 Cell Line	embryonic stem cell
3	chr1:222819200-222841400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:222819200-222841600	Strong transcription	Placenta	Placenta
5	chr1:222819400-222841200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr1:222820000-222838800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:222820000-222841400	Strong transcription	HSMM	muscle
8	chr1:222820000-222841600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:222820200-222838800	Strong transcription	NHDF-Ad	bronchial
10	chr1:222820200-222841400	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:222820200-222841400	Strong transcription	NH-A	brain
12	chr1:222820400-222841800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:222820600-222841200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr1:222820600-222841400	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr1:222820800-222841000	Strong transcription	Skeletal Muscle Female	skeletal muscle
16	chr1:222820800-222841200	Strong transcription	Fetal Intestine Large	intestine
17	chr1:222821000-222840000	Strong transcription	Fetal Kidney	kidney
18	chr1:222821200-222841400	Strong transcription	Adipose Nuclei	Adipose
19	chr1:222821400-222840000	Strong transcription	Fetal Brain Female	brain
20	chr1:222822200-222838800	Strong transcription	Colon Smooth Muscle	Colon
21	chr1:222822200-222841200	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:222822200-222841400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:222822400-222841200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:222822400-222841400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr1:222822600-222840000	Strong transcription	Fetal Muscle Trunk	muscle
26	chr1:222822600-222841400	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr1:222822600-222841400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr1:222822800-222840800	Strong transcription	Stomach Smooth Muscle	stomach
29	chr1:222823000-222838400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:222823000-222839200	Strong transcription	Fetal Muscle Leg	muscle
31	chr1:222823000-222841200	Strong transcription	H1 Cell Line	embryonic stem cell
32	chr1:222823000-222841400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr1:222823200-222840000	Strong transcription	Brain Substantia Nigra	brain
34	chr1:222823200-222840600	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr1:222823200-222841400	Strong transcription	HepG2	liver
36	chr1:222823200-222841400	Strong transcription	K562	blood
37	chr1:222823400-222841400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:222824000-222839600	Strong transcription	Skeletal Muscle Male	skeletal muscle
39	chr1:222824000-222841400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr1:222824000-222841400	Strong transcription	A549	lung
41	chr1:222824200-222839800	Strong transcription	Fetal Lung	lung
42	chr1:222825000-222841400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:222825200-222839000	Strong transcription	Brain Cingulate Gyrus	brain
44	chr1:222825600-222840000	Strong transcription	Left Ventricle	heart
45	chr1:222825800-222839600	Strong transcription	Rectal Smooth Muscle	rectum
46	chr1:222826800-222841400	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr1:222827000-222835400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr1:222827000-222838000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr1:222827000-222845400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:222827200-222835400	Weak transcription	Aorta	Aorta

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