Variant report

Variant	rs17155405
Chromosome Location	chr7:107947475-107947476
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:107945991..107948006-chr7:107951192..107954183,2	MCF-7	breast:
2	chr7:107946487..107948369-chr7:107949366..107951940,2	K562	blood:
3	chr7:107945282..107948369-chr7:107949981..107952858,4	K562	blood:
4	chr7:107934726..107936588-chr7:107945741..107947736,2	K562	blood:

Variant related genes	Relation type
ENSG00000091129	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10487841	0.82[CEU][hapmap]
rs12534519	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12537209	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs16872497	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.95[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs16872512	1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[JPT][hapmap]
rs16872515	0.83[GIH][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap]
rs16872517	1.00[CEU][hapmap];0.92[CHB][hapmap];0.86[CHD][hapmap];0.89[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.95[AMR][1000 genomes]
rs17134752	0.82[CEU][hapmap]
rs17155397	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17155446	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17155536	0.86[AMR][1000 genomes]
rs17155579	0.82[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap]
rs17155592	1.00[CEU][hapmap];0.92[CHB][hapmap];0.91[CHD][hapmap];0.83[GIH][hapmap];0.89[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.95[AMR][1000 genomes]
rs17155613	0.82[CEU][hapmap];0.92[CHB][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap]
rs17155617	0.82[CEU][hapmap];0.92[CHB][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap]
rs17329871	1.00[CEU][hapmap]
rs17330779	1.00[CEU][hapmap]
rs17388677	1.00[CEU][hapmap]
rs17388872	1.00[CEU][hapmap]
rs17420235	1.00[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap]
rs2024491	0.86[AMR][1000 genomes]
rs2193243	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs2300020	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2300031	0.81[AMR][1000 genomes]
rs367668	0.82[CEU][hapmap]
rs56100765	0.82[AMR][1000 genomes]
rs59164222	0.86[AMR][1000 genomes]
rs6944131	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6973148	0.82[CEU][hapmap]
rs73420238	0.86[AMR][1000 genomes]
rs7792869	1.00[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap];0.95[AMR][1000 genomes]
rs7792996	0.82[CEU][hapmap]
rs7794233	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.84[TSI][hapmap];0.86[AMR][1000 genomes]
rs7811595	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7812138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
2	nsv949344	chr7:107396502-107987085	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv831090	chr7:107786650-108011196	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
4	nsv888942	chr7:107893695-108055858	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv888943	chr7:107893695-108058574	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	nsv1030425	chr7:107910716-108041036	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv1019059	chr7:107935905-107995523	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	nsv1021783	chr7:107935905-107998281	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	esv2761354	chr7:107935905-107998293	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv1031824	chr7:107935905-108006038	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	nsv1017288	chr7:107939739-108000837	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 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	chr7:107925400-107952000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:107932000-107950600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:107935400-107950600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr7:107940400-107947600	Weak transcription	Brain Substantia Nigra	brain
5	chr7:107940400-107964400	Weak transcription	Pancreas	Pancrea
6	chr7:107943000-107947600	Weak transcription	Brain Angular Gyrus	brain
7	chr7:107943000-107948400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:107943200-107947600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:107943200-107948200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:107944600-107947800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:107945400-107953800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:107945600-107954000	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr7:107945800-107947800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:107945800-107952600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:107945800-107954000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:107945800-107956000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:107946200-107947600	Weak transcription	Brain Anterior Caudate	brain
18	chr7:107946200-107947600	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr7:107946200-107947600	Weak transcription	A549	lung
20	chr7:107947000-107949000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:107947000-107949400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:107947000-107953800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr7:107947200-107948600	Enhancers	Fetal Brain Male	brain
24	chr7:107947200-107948800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:107947200-107951400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:107947400-107948000	Enhancers	Brain Hippocampus Middle	brain
27	chr7:107947400-107948000	Enhancers	Fetal Brain Female	brain
28	chr7:107947400-107951000	Enhancers	Brain Cingulate Gyrus	brain

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