Variant report

Variant	rs6910157
Chromosome Location	chr6:147317778-147317779
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:147312426..147314178-chr6:147315717..147317793,2	K562	blood:
2	chr6:147316468..147318660-chr6:147533860..147536236,2	K562	blood:
3	chr6:147316757..147318385-chr6:147332392..147334165,2	K562	blood:
4	chr6:147316176..147319169-chr6:147524425..147526437,2	K562	blood:
5	chr6:147315835..147318626-chr6:147323386..147326215,2	K562	blood:

Variant related genes	Relation type
ENSG00000164506	Chromatin interaction
ENSG00000233452	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10499242	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10499244	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10499245	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11966340	0.97[ASN][1000 genomes]
rs11966941	0.97[ASN][1000 genomes]
rs12660458	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12661319	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12662397	0.93[ASN][1000 genomes]
rs12663509	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12664925	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12665457	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12665594	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12665649	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17076435	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17076442	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17076444	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17076452	0.83[ASN][1000 genomes]
rs17076474	0.93[ASN][1000 genomes]
rs17076499	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17076505	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17076507	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17076510	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17076512	0.93[ASN][1000 genomes]
rs17076522	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17076531	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17076533	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17076538	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17076540	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1852797	0.93[ASN][1000 genomes]
rs58553228	0.83[ASN][1000 genomes]
rs6915087	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147311400-147321200	Weak transcription	HSMM	muscle
2	chr6:147311800-147318000	Weak transcription	NHLF	lung
3	chr6:147312600-147318000	Weak transcription	NH-A	brain
4	chr6:147312600-147318400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:147312600-147321000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:147312800-147318000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:147312800-147318200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr6:147313000-147318000	Weak transcription	Osteobl	bone
9	chr6:147313400-147318000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:147313400-147318000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr6:147313400-147318200	Weak transcription	NHDF-Ad	bronchial
12	chr6:147313400-147320800	Weak transcription	K562	blood
13	chr6:147313600-147318000	Weak transcription	A549	lung
14	chr6:147313800-147318400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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