Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:103967859..103969878-chr12:103972890..103976070,3	K562	blood:
2	chr12:103974772..103977268-chr12:103979436..103981472,2	K562	blood:

Variant related genes	Relation type
ENSG00000136011	Chromatin interaction

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10745973	0.98[ASN][1000 genomes]
rs10745974	0.98[ASN][1000 genomes]
rs10778263	0.93[ASN][1000 genomes]
rs10778264	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10861041	0.98[ASN][1000 genomes]
rs12832814	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1346411	0.93[ASN][1000 genomes]
rs1593810	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1593811	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1593812	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17034119	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17034127	0.89[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17034172	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17034187	1.00[EUR][1000 genomes]
rs35929067	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4131522	0.93[ASN][1000 genomes]
rs4237987	0.99[ASN][1000 genomes]
rs4388997	0.92[ASN][1000 genomes]
rs4764966	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs56402195	1.00[EUR][1000 genomes]
rs6539082	0.97[ASN][1000 genomes]
rs67057049	0.96[ASN][1000 genomes]
rs7311417	0.97[ASN][1000 genomes]
rs7953892	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs7955950	0.91[ASN][1000 genomes]
rs7979954	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103974200-103976400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:103974200-103976800	Weak transcription	HMEC	breast
3	chr12:103974200-103977000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr12:103975000-103976000	Weak transcription	NHEK	skin
5	chr12:103975000-103976800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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