Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:127257978..127262943-chr5:127415784..127421768,10	MCF-7	breast:
2	chr5:127261908..127263560-chr5:127300086..127302066,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000064651	Chromatin interaction
ENSG00000245937	Chromatin interaction

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

rs_ID	r²[population]
rs10052229	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10071108	0.81[ASN][1000 genomes]
rs10477678	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12654649	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17164505	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2263502	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2409034	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2409035	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2409036	0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2681509	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4836341	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4836343	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56806325	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6865186	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6898966	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73331900	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7711172	0.86[EUR][1000 genomes];0.88[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	nsv1033607	chr5:126385181-127304459	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1021483	chr5:126927834-127304873	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv3327104	chr5:127261911-127262146	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:127253000-127266200	Weak transcription	Fetal Heart	heart
2	chr5:127258200-127262200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr5:127258400-127266400	Weak transcription	Gastric	stomach
4	chr5:127258400-127266400	Weak transcription	Pancreas	Pancrea
5	chr5:127259400-127262400	Enhancers	A549	lung
6	chr5:127260000-127262400	Weak transcription	GM12878-XiMat	blood
7	chr5:127260600-127265600	Weak transcription	HUVEC	blood vessel
8	chr5:127261000-127262200	Enhancers	HMEC	breast
9	chr5:127261200-127262600	Enhancers	Stomach Mucosa	stomach
10	chr5:127261200-127266000	Weak transcription	HSMMtube	muscle
11	chr5:127261400-127262200	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr5:127261400-127262400	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr5:127261800-127262600	Enhancers	Fetal Intestine Large	intestine
14	chr5:127261800-127266000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:127261800-127266200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:127261800-127270200	Weak transcription	NHEK	skin
17	chr5:127262000-127262600	Enhancers	Duodenum Mucosa	Duodenum
18	chr5:127262000-127262800	Enhancers	Fetal Intestine Small	intestine
19	chr5:127262000-127262800	Enhancers	Small Intestine	intestine
20	chr5:127262000-127266200	Weak transcription	Hela-S3	cervix

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