Variant report

Variant	rs72702685
Chromosome Location	chr9:12856919-12856920
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10491739	0.83[AMR][1000 genomes]
rs10491740	0.82[AMR][1000 genomes]
rs10960819	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13285285	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13291898	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16923061	0.80[AMR][1000 genomes]
rs16929646	0.80[ASN][1000 genomes]
rs16929698	0.86[ASN][1000 genomes]
rs56728829	0.97[ASN][1000 genomes]
rs61536442	0.81[AMR][1000 genomes]
rs66647545	0.97[ASN][1000 genomes]
rs67301291	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs67463684	0.86[ASN][1000 genomes]
rs68187573	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7043074	0.84[AMR][1000 genomes]
rs7868380	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498136	chr9:12387840-12984158	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv2422212	chr9:12448789-13127738	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv892573	chr9:12730636-12874703	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers 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	10 gene(s)	inside rSNPs	diseases
4	nsv892574	chr9:12754969-12918226	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv613615	chr9:12830070-12947238	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12850400-12859200	Weak transcription	Small Intestine	intestine
2	chr9:12850600-12859000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr9:12851000-12858400	Weak transcription	Stomach Mucosa	stomach
4	chr9:12851800-12867000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr9:12854600-12859200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:12854800-12859400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:12854800-12859400	Weak transcription	Fetal Intestine Large	intestine
8	chr9:12854800-12860000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr9:12855000-12859200	Weak transcription	Fetal Intestine Small	intestine
10	chr9:12855200-12857200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr9:12855200-12859600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr9:12855400-12857800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr9:12855400-12858200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:12855400-12858400	Weak transcription	HMEC	breast
15	chr9:12855600-12857200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr9:12855600-12858800	Weak transcription	NHEK	skin
17	chr9:12855600-12859400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:12855600-12859600	Weak transcription	Adipose Nuclei	Adipose
19	chr9:12856000-12857000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr9:12856000-12857200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr9:12856400-12857000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr9:12856400-12857000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr9:12856400-12857200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr9:12856400-12857200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr9:12856400-12857200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr9:12856400-12857200	Enhancers	Fetal Lung	lung
27	chr9:12856600-12857000	Enhancers	Fetal Kidney	kidney
28	chr9:12856600-12857200	Enhancers	Fetal Stomach	stomach
29	chr9:12856800-12857000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr9:12856800-12857200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr9:12856800-12860000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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