Variant report

Variant	rs7785246
Chromosome Location	chr7:139542174-139542175
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:139539840..139543405-chr7:139545009..139547964,3	K562	blood:
2	chr7:139532720..139535197-chr7:139540862..139542480,2	K562	blood:
3	chr7:139541194..139543649-chr7:139594148..139596879,2	K562	blood:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10487662	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17178226	1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17178522	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17178543	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs56317504	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6953224	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs73733507	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7801524	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8192805	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]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020234	chr7:139377822-139661964	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1032711	chr7:139411404-139684043	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv464732	chr7:139424022-139654256	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv608472	chr7:139424022-139654256	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1018712	chr7:139429703-139658014	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv831156	chr7:139532318-139694326	Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:139531400-139542200	Weak transcription	Spleen	Spleen
2	chr7:139531400-139544600	Weak transcription	Gastric	stomach
3	chr7:139531400-139553800	Weak transcription	Primary T cells from cord blood	blood
4	chr7:139531400-139572600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr7:139531600-139542400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:139540600-139545000	Genic enhancers	Primary monocytes fromperipheralblood	blood
7	chr7:139540800-139542200	Weak transcription	Lung	lung
8	chr7:139540800-139544400	Weak transcription	Pancreas	Pancrea
9	chr7:139540800-139544800	Weak transcription	Esophagus	oesophagus
10	chr7:139541000-139555200	Weak transcription	Thymus	Thymus
11	chr7:139541200-139542800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:139541200-139543000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:139541400-139543000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:139541600-139542400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
15	chr7:139541600-139543000	Enhancers	Fetal Kidney	kidney
16	chr7:139541800-139542200	Active TSS	Duodenum Mucosa	Duodenum
17	chr7:139541800-139542200	Enhancers	GM12878-XiMat	blood
18	chr7:139541800-139542200	Active TSS	NHLF	lung
19	chr7:139541800-139542400	Active TSS	Adipose Nuclei	Adipose
20	chr7:139541800-139542800	Enhancers	Primary hematopoietic stem cells	blood
21	chr7:139541800-139542800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:139541800-139543000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr7:139541800-139543000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr7:139542000-139542400	Enhancers	Fetal Lung	lung
25	chr7:139542000-139542400	Active TSS	Ovary	ovary
26	chr7:139542000-139542400	Active TSS	Right Atrium	heart
27	chr7:139542000-139542400	Enhancers	HepG2	liver
28	chr7:139542000-139542600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:139542000-139542600	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr7:139542000-139542600	Enhancers	Placenta	Placenta
31	chr7:139542000-139542600	Enhancers	Hela-S3	cervix
32	chr7:139542000-139543200	Enhancers	Primary B cells from peripheral blood	blood
33	chr7:139542000-139543200	Enhancers	Fetal Thymus	thymus

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