Variant report

Variant	rs61616797
Chromosome Location	chr11:73589730-73589731
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:73561146..73563311-chr11:73588199..73589761,2	K562	blood:
2	chr11:73101451..73103302-chr11:73587436..73589979,2	MCF-7	breast:
3	chr11:73587462..73590069-chr11:73692817..73694652,2	K562	blood:

Variant related genes	Relation type
ENSG00000054967	Chromatin interaction
ENSG00000175567	Chromatin interaction
ENSG00000256681	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11821823	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11822264	1.00[EUR][1000 genomes]
rs11822794	1.00[EUR][1000 genomes]
rs11823400	1.00[EUR][1000 genomes]
rs11824937	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11825819	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11826017	1.00[EUR][1000 genomes]
rs11827951	1.00[EUR][1000 genomes]
rs11828393	1.00[EUR][1000 genomes]
rs11829005	1.00[EUR][1000 genomes]
rs11829012	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17132408	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17132421	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17132422	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17132438	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17132488	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17132555	1.00[EUR][1000 genomes]
rs45476292	1.00[EUR][1000 genomes]
rs45570334	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55840703	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55893487	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55939206	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56117405	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56168571	0.87[AMR][1000 genomes]
rs56237750	1.00[EUR][1000 genomes]
rs56340309	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56378817	1.00[EUR][1000 genomes]
rs56723437	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56767203	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57579114	1.00[EUR][1000 genomes]
rs58792356	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59621450	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60093210	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60520592	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60924318	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61085412	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61581672	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61701946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7110607	1.00[EUR][1000 genomes]
rs73543094	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530624	chr11:73114283-73646329	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv492091	chr11:73285970-73844424	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
3	nsv530641	chr11:73358393-73638725	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv1038105	chr11:73552023-73673836	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv1035977	chr11:73581224-73617653	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73588600-73590000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
2	chr11:73588600-73591000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:73588600-73591000	Weak transcription	Esophagus	oesophagus
4	chr11:73588600-73594800	Weak transcription	Ovary	ovary
5	chr11:73588600-73599400	Weak transcription	Left Ventricle	heart
6	chr11:73588600-73610200	Weak transcription	Gastric	stomach
7	chr11:73588600-73610200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr11:73588600-73611200	Weak transcription	Aorta	Aorta
9	chr11:73588800-73589800	Weak transcription	Stomach Mucosa	stomach
10	chr11:73588800-73590000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr11:73588800-73590000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr11:73588800-73590000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr11:73588800-73590000	Enhancers	Fetal Intestine Large	intestine
14	chr11:73588800-73590800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr11:73588800-73590800	Weak transcription	Fetal Stomach	stomach
16	chr11:73588800-73590800	Weak transcription	Pancreas	Pancrea
17	chr11:73588800-73591000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:73588800-73594400	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr11:73588800-73594400	Weak transcription	Fetal Brain Female	brain
20	chr11:73588800-73594600	Weak transcription	Placenta	Placenta
21	chr11:73588800-73594800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:73588800-73594800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr11:73588800-73595000	Weak transcription	Thymus	Thymus
24	chr11:73588800-73595200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr11:73588800-73597000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr11:73588800-73597800	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr11:73588800-73598000	Weak transcription	Primary B cells from peripheral blood	blood
28	chr11:73588800-73598200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr11:73588800-73598400	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr11:73588800-73598400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr11:73588800-73598400	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr11:73588800-73599400	Weak transcription	Fetal Heart	heart
33	chr11:73588800-73599400	Weak transcription	Psoas Muscle	Psoas
34	chr11:73588800-73599400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr11:73588800-73599400	Weak transcription	HSMMtube	muscle
36	chr11:73588800-73599800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr11:73588800-73599800	Weak transcription	Colon Smooth Muscle	Colon
38	chr11:73588800-73599800	Weak transcription	NHLF	lung
39	chr11:73588800-73600000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr11:73588800-73600000	Weak transcription	HMEC	breast
41	chr11:73588800-73600000	Weak transcription	NHDF-Ad	bronchial
42	chr11:73588800-73600200	Weak transcription	Brain Angular Gyrus	brain
43	chr11:73588800-73600200	Weak transcription	NH-A	brain
44	chr11:73588800-73600600	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr11:73588800-73600800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr11:73588800-73604200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr11:73588800-73604800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr11:73588800-73606200	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr11:73588800-73607000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr11:73588800-73610200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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