Variant report

Variant	rs883016
Chromosome Location	chr10:50217522-50217523
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	chr10:50217414..50220289-chr10:50222557..50225109,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12569955	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap]
rs2246796	1.00[GIH][hapmap]
rs2254632	0.90[CHB][hapmap];1.00[CHD][hapmap]
rs2254861	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2255134	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2255357	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2255379	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2255486	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2264845	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2943252	0.90[CHB][hapmap];0.92[CHD][hapmap]
rs57192152	0.91[ASN][1000 genomes]
rs57195574	1.00[ASN][1000 genomes]
rs58468873	0.89[ASN][1000 genomes]
rs59250742	0.89[ASN][1000 genomes]
rs59443750	0.89[ASN][1000 genomes]
rs60282422	0.91[ASN][1000 genomes]
rs61403024	1.00[ASN][1000 genomes]
rs7080920	1.00[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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831866	chr10:50165180-50335276	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
3	nsv6620	chr10:50197344-50224635	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50210800-50219800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:50210800-50223600	Weak transcription	Spleen	Spleen
3	chr10:50213400-50223000	Enhancers	Ovary	ovary
4	chr10:50215000-50219400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr10:50215200-50218400	Enhancers	Fetal Brain Male	brain
6	chr10:50215200-50222400	Enhancers	Left Ventricle	heart
7	chr10:50215400-50219400	Enhancers	Fetal Stomach	stomach
8	chr10:50216000-50218000	Enhancers	Fetal Lung	lung
9	chr10:50216000-50218800	Enhancers	Right Atrium	heart
10	chr10:50216000-50219800	Enhancers	Fetal Muscle Trunk	muscle
11	chr10:50216000-50219800	Enhancers	Fetal Muscle Leg	muscle
12	chr10:50216200-50217800	Enhancers	HSMMtube	muscle
13	chr10:50216200-50220000	Enhancers	Fetal Intestine Large	intestine
14	chr10:50216200-50221800	Enhancers	Fetal Intestine Small	intestine
15	chr10:50216400-50217600	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr10:50216600-50218200	Enhancers	Fetal Heart	heart
17	chr10:50216600-50218600	Weak transcription	Colon Smooth Muscle	Colon
18	chr10:50216600-50219000	Enhancers	K562	blood
19	chr10:50216600-50222000	Enhancers	Right Ventricle	heart
20	chr10:50216600-50223000	Enhancers	Placenta	Placenta
21	chr10:50216800-50218400	Weak transcription	Esophagus	oesophagus
22	chr10:50216800-50218400	Enhancers	Fetal Brain Female	brain
23	chr10:50217000-50218600	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr10:50217200-50217600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr10:50217200-50217600	Flanking Active TSS	Stomach Smooth Muscle	stomach
26	chr10:50217200-50219200	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr10:50217200-50220600	Weak transcription	Brain Hippocampus Middle	brain
28	chr10:50217200-50226600	Weak transcription	Aorta	Aorta
29	chr10:50217400-50217600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr10:50217400-50218200	Enhancers	Adipose Nuclei	Adipose
31	chr10:50217400-50218400	Weak transcription	Psoas Muscle	Psoas
32	chr10:50217400-50231200	Weak transcription	Rectal Smooth Muscle	rectum

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