Variant report

Variant	rs73416707
Chromosome Location	chr7:112626934-112626935
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:112609190..112612964-chr7:112622640..112627113,4	K562	blood:

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs73416712	0.95[AFR][1000 genomes];1.00[AMR][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	esv2758131	chr7:112492127-112768628	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv2759556	chr7:112492127-112768628	Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3355135	chr7:112616979-113134651	Active TSS Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv435847	chr7:112618576-113134022	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv3430638	chr7:112620663-113134403	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv3442221	chr7:112620665-113134971	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv993501	chr7:112625029-113125338	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112594200-112630400	Weak transcription	Left Ventricle	heart
2	chr7:112622400-112627800	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr7:112625000-112629000	Enhancers	HMEC	breast
4	chr7:112625000-112631200	Enhancers	Fetal Heart	heart
5	chr7:112625600-112627400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
6	chr7:112625600-112627400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr7:112625600-112627800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:112625600-112627800	Enhancers	NHDF-Ad	bronchial
9	chr7:112625600-112628200	Enhancers	HSMM	muscle
10	chr7:112625800-112628600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:112625800-112629200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:112626000-112627000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr7:112626000-112627800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:112626200-112627000	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr7:112626200-112627000	Enhancers	Colon Smooth Muscle	Colon
16	chr7:112626200-112628400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr7:112626200-112628400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:112626400-112628600	Enhancers	Osteobl	bone
19	chr7:112626600-112627200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr7:112626600-112627200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:112626600-112627200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:112626600-112628400	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr7:112626600-112628600	Enhancers	NHLF	lung
24	chr7:112626600-112628800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr7:112626800-112627000	Enhancers	HSMMtube	muscle
26	chr7:112626800-112628400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:112626800-112628600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:112626800-112630400	Weak transcription	NHEK	skin
29	chr7:112626800-112631400	Enhancers	NH-A	brain

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