Variant report

Variant	rs6697116
Chromosome Location	chr1:186910419-186910420
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	chr1:186344989..186347809-chr1:186910086..186912699,2	K562	blood:

Variant related genes	Relation type
ENSG00000157181	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10911972	0.91[ASN][1000 genomes]
rs2891261	0.91[ASN][1000 genomes]
rs4276871	0.91[ASN][1000 genomes]
rs5027750	0.91[ASN][1000 genomes]
rs59300656	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60979573	0.93[ASN][1000 genomes]
rs61208933	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6675166	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6675898	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6678709	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6688358	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs66896520	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6698103	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67334743	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67896462	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72641703	0.89[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7526761	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872590	chr1:186557453-187500338	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv548407	chr1:186875459-186951429	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186881800-186933600	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr1:186881800-186951200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr1:186890000-186924400	Weak transcription	Fetal Stomach	stomach
4	chr1:186890800-186928400	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr1:186892800-186924000	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr1:186895400-186937000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr1:186897600-186917800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:186897600-186920800	Weak transcription	Fetal Intestine Small	intestine
9	chr1:186900000-186935800	Weak transcription	NHDF-Ad	bronchial
10	chr1:186902600-186911000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:186904000-186925200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr1:186906600-186910600	Strong transcription	Primary hematopoietic stem cells	blood
13	chr1:186906600-186920800	Weak transcription	Fetal Intestine Large	intestine
14	chr1:186907200-186911400	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr1:186907600-186911000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr1:186908000-186933800	Weak transcription	Colon Smooth Muscle	Colon
17	chr1:186909800-186911400	Weak transcription	Hela-S3	cervix
18	chr1:186909800-186916400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:186909800-186922600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr1:186909800-186932600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr1:186910000-186920000	Weak transcription	Adipose Nuclei	Adipose
22	chr1:186910400-186911800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:186910400-186917600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:186910400-186919000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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