Variant report

Variant	rs7805497
Chromosome Location	chr7:27950339-27950340
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10232181	0.81[EUR][1000 genomes]
rs10236987	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs10239787	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs10244184	0.80[CEU][hapmap]
rs10244948	1.00[CHB][hapmap]
rs10248465	1.00[CHB][hapmap]
rs10250533	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10275982	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10278615	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10282662	1.00[CHB][hapmap]
rs10951188	1.00[CHB][hapmap]
rs12531234	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13226126	0.91[CEU][hapmap];0.95[EUR][1000 genomes]
rs13236531	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1557780	1.00[CHB][hapmap]
rs28507096	0.83[ASN][1000 genomes]
rs35135622	1.00[ASN][1000 genomes]
rs4722745	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs56410344	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs67583972	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7787576	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs7804500	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7804617	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv949025	chr7:27578167-28075172	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2758109	chr7:27793616-27972869	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	esv2759520	chr7:27793616-27972869	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv1030685	chr7:27844038-28177301	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1024819	chr7:27949955-28020969	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27926600-27956000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:27937600-27953800	Weak transcription	Right Ventricle	heart
3	chr7:27937600-27956200	Weak transcription	Gastric	stomach
4	chr7:27939200-27953000	Weak transcription	Left Ventricle	heart
5	chr7:27939800-27950400	Weak transcription	Pancreas	Pancrea
6	chr7:27941200-27954400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr7:27941200-27956200	Weak transcription	Aorta	Aorta
8	chr7:27941400-27957600	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:27941400-27990800	Weak transcription	Primary T cells from cord blood	blood
10	chr7:27941600-27956000	Weak transcription	Brain Hippocampus Middle	brain
11	chr7:27941600-27962800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr7:27942200-27953800	Weak transcription	Stomach Smooth Muscle	stomach
13	chr7:27942200-27956000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr7:27942400-27952400	Weak transcription	Primary B cells from cord blood	blood
15	chr7:27942400-28005600	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr7:27946000-27952400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:27946600-27953400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr7:27946800-27953400	Weak transcription	Colon Smooth Muscle	Colon
19	chr7:27947600-27950400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:27949000-27957400	Weak transcription	Primary B cells from peripheral blood	blood
21	chr7:27949200-27952600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr7:27949400-27950600	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr7:27949400-27951200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:27949400-27954400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr7:27949600-27950400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:27949600-27950400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:27949600-27950400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr7:27949600-27950600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:27949600-27950600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:27949600-27950600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr7:27949600-27950600	Enhancers	HSMMtube	muscle
32	chr7:27949600-27950600	Enhancers	Osteobl	bone
33	chr7:27949600-27950800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr7:27949600-27952200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr7:27949600-27953200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr7:27949600-27953400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr7:27949600-27955200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:27949800-27950400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:27949800-27950400	Enhancers	NH-A	brain
40	chr7:27949800-27950600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:27949800-27950600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr7:27949800-27950600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:27949800-27950600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr7:27949800-27950600	Enhancers	NHDF-Ad	bronchial
45	chr7:27949800-27950800	Enhancers	Brain Germinal Matrix	brain
46	chr7:27949800-27952600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr7:27950000-27950400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr7:27950000-27950400	Enhancers	Fetal Brain Female	brain
49	chr7:27950000-27950600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr7:27950200-27950400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell

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