Variant report

Variant	rs7755403
Chromosome Location	chr6:24453447-24453448
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:24450784..24454394-chr6:24459260..24463305,3	K562	blood:
2	chr6:24391794..24393739-chr6:24451484..24453982,2	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs2295649	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs2744565	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2793430	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2793431	0.83[ASN][1000 genomes]
rs2793437	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs793671	0.82[CEU][hapmap]
rs9358767	0.84[ASN][1000 genomes]
rs9393556	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9393557	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9393558	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026638	chr6:24347972-24475300	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases
2	esv2763542	chr6:24445131-24520637	Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv519552	chr6:24451256-24524704	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24421200-24459600	Weak transcription	Spleen	Spleen
2	chr6:24424000-24456600	Weak transcription	Ovary	ovary
3	chr6:24427600-24456800	Weak transcription	Lung	lung
4	chr6:24427800-24467000	Weak transcription	Brain Germinal Matrix	brain
5	chr6:24429000-24494200	Weak transcription	Primary B cells from cord blood	blood
6	chr6:24429200-24455600	Weak transcription	Brain Angular Gyrus	brain
7	chr6:24429400-24483800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr6:24429600-24455000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:24432600-24463800	Weak transcription	Fetal Intestine Small	intestine
10	chr6:24437600-24455400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:24437800-24459600	Weak transcription	Left Ventricle	heart
12	chr6:24438000-24464000	Weak transcription	Pancreas	Pancrea
13	chr6:24438200-24455600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr6:24438400-24483200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:24438600-24459800	Weak transcription	Fetal Stomach	stomach
16	chr6:24438800-24469200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr6:24444000-24458200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr6:24447200-24470200	Weak transcription	Aorta	Aorta
19	chr6:24447400-24490400	Weak transcription	Brain Anterior Caudate	brain
20	chr6:24448200-24466200	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr6:24448400-24458000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr6:24448800-24488000	Weak transcription	Fetal Muscle Leg	muscle
23	chr6:24450200-24459400	Weak transcription	Esophagus	oesophagus
24	chr6:24452000-24453600	Enhancers	Thymus	Thymus
25	chr6:24452200-24458400	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr6:24452400-24458200	Weak transcription	Adipose Nuclei	Adipose
27	chr6:24452600-24466400	Weak transcription	Dnd41	blood
28	chr6:24452800-24458400	Weak transcription	Hela-S3	cervix
29	chr6:24453200-24471000	Strong transcription	Liver	Liver
30	chr6:24453400-24454400	Weak transcription	Fetal Thymus	thymus

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