Variant report

Variant	rs11111815
Chromosome Location	chr12:104248787-104248788
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:104233313..104235106-chr12:104245857..104249514,3	MCF-7	breast:
2	chr12:104233205..104236875-chr12:104247601..104251045,3	MCF-7	breast:
3	chr12:104242967..104244745-chr12:104247327..104248982,2	K562	blood:
4	chr12:104232946..104237794-chr12:104239535..104249085,16	K562	blood:
5	chr12:104247921..104249635-chr12:104251344..104253746,2	MCF-7	breast:
6	chr12:104247941..104249530-chr12:104249727..104251243,2	K562	blood:
7	chr12:104244166..104246985-chr12:104247469..104250168,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000257327	Chromatin interaction
ENSG00000111696	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10745984	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10778292	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10861130	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10861131	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10861142	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10861143	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10861146	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs11111821	0.86[EUR][1000 genomes]
rs11111831	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12302488	0.91[CEU][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12369947	0.91[CEU][hapmap]
rs12371102	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17034938	0.91[CEU][hapmap]
rs2576969	0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs3812801	0.89[ASW][hapmap];0.91[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MKK][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4135138	1.00[JPT][hapmap]
rs6539103	0.95[ASN][1000 genomes]
rs7302036	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7968124	0.95[ASN][1000 genomes]
rs7971317	0.95[ASN][1000 genomes]
rs7971563	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9308316	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs9989004	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[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	esv34031	chr12:104114277-104298546	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv560039	chr12:104177668-104455340	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104236000-104252600	Weak transcription	Esophagus	oesophagus
2	chr12:104236000-104252600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr12:104236000-104253600	Weak transcription	Gastric	stomach
4	chr12:104240000-104254800	Enhancers	Rectal Smooth Muscle	rectum
5	chr12:104243800-104251400	Enhancers	Colon Smooth Muscle	Colon
6	chr12:104245000-104250800	Enhancers	HepG2	liver
7	chr12:104245200-104252000	Enhancers	Stomach Smooth Muscle	stomach
8	chr12:104245600-104249400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr12:104246400-104252600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr12:104246600-104249000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr12:104246600-104252400	Weak transcription	NHEK	skin
12	chr12:104246600-104253200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:104246800-104248800	Weak transcription	NH-A	brain
14	chr12:104246800-104249000	Weak transcription	HSMM	muscle
15	chr12:104246800-104249000	Weak transcription	Osteobl	bone
16	chr12:104246800-104249200	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr12:104246800-104249200	Weak transcription	HMEC	breast
18	chr12:104246800-104251000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr12:104246800-104251400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr12:104246800-104252200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:104246800-104254000	Weak transcription	Brain Anterior Caudate	brain
22	chr12:104247000-104248800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr12:104247600-104249000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr12:104247600-104249200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr12:104247600-104250000	Enhancers	Pancreas	Pancrea
26	chr12:104247800-104252200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:104248000-104248800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:104248200-104250000	Enhancers	Liver	Liver
29	chr12:104248400-104248800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:104248400-104248800	Enhancers	Fetal Stomach	stomach

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