Variant report

Variant	rs11822234
Chromosome Location	chr11:74385146-74385147
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:74382546..74386046-chr11:74386677..74389972,4	K562	blood:
2	chr11:74377887..74381044-chr11:74384052..74387335,4	K562	blood:
3	chr11:74383555..74386388-chr11:74394494..74397329,2	K562	blood:
4	chr11:74384288..74386885-chr11:74391965..74393932,2	K562	blood:
5	chr11:74354455..74356432-chr11:74382989..74385315,2	K562	blood:

Variant related genes	Relation type
ENSG00000223202	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10899031	0.81[ASN][1000 genomes]
rs11602237	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17244949	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6592590	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7104802	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7129492	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757451	chr11:73842609-74545888	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	esv2759837	chr11:73842609-74557597	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	esv34979	chr11:73878688-74533452	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
4	esv2758277	chr11:73887567-74557597	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
5	nsv825994	chr11:73936667-74534455	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
6	nsv932190	chr11:74359867-74618935	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74369200-74385400	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr11:74372000-74393000	Weak transcription	Fetal Brain Female	brain
3	chr11:74381400-74385600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:74381400-74386000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:74381600-74394000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:74382400-74385400	Enhancers	Fetal Muscle Leg	muscle
7	chr11:74382600-74385200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr11:74382600-74385200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr11:74382600-74385200	Enhancers	HSMMtube	muscle
10	chr11:74382600-74385200	Enhancers	NHDF-Ad	bronchial
11	chr11:74382600-74385400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr11:74382600-74385400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr11:74382600-74385400	Enhancers	NHLF	lung
14	chr11:74382800-74385200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr11:74382800-74385200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr11:74382800-74385200	Enhancers	HMEC	breast
17	chr11:74382800-74385400	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr11:74383000-74385200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr11:74383200-74385200	Flanking Active TSS	Hela-S3	cervix
20	chr11:74383400-74385200	Enhancers	Brain Angular Gyrus	brain
21	chr11:74383400-74385200	Enhancers	Brain Anterior Caudate	brain
22	chr11:74383400-74385200	Enhancers	Brain Germinal Matrix	brain
23	chr11:74383400-74385400	Enhancers	Brain Substantia Nigra	brain
24	chr11:74383400-74385400	Enhancers	Fetal Stomach	stomach
25	chr11:74383400-74385400	Enhancers	Rectal Smooth Muscle	rectum
26	chr11:74383600-74385200	Enhancers	Brain Cingulate Gyrus	brain
27	chr11:74383600-74385200	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr11:74384000-74387600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:74384200-74385200	Flanking Active TSS	Brain Hippocampus Middle	brain
30	chr11:74384200-74392400	Weak transcription	Right Ventricle	heart
31	chr11:74384400-74385200	Flanking Active TSS	A549	lung
32	chr11:74384400-74392600	Weak transcription	Psoas Muscle	Psoas
33	chr11:74384400-74394200	Weak transcription	Lung	lung
34	chr11:74384600-74387600	Weak transcription	Fetal Muscle Trunk	muscle
35	chr11:74384800-74385200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr11:74384800-74385400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr11:74384800-74385400	Enhancers	Stomach Smooth Muscle	stomach
38	chr11:74384800-74385400	Enhancers	HSMM	muscle
39	chr11:74384800-74385400	Enhancers	NH-A	brain
40	chr11:74384800-74387600	Weak transcription	Ovary	ovary
41	chr11:74384800-74388400	Weak transcription	Pancreas	Pancrea
42	chr11:74384800-74392000	Weak transcription	Placenta	Placenta
43	chr11:74384800-74392200	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr11:74384800-74392600	Weak transcription	Spleen	Spleen
45	chr11:74384800-74394200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr11:74385000-74385200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:74385000-74385200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr11:74385000-74385200	Enhancers	K562	blood
49	chr11:74385000-74385400	Enhancers	Muscle Satellite Cultured Cells	--
50	chr11:74385000-74385400	Enhancers	Osteobl	bone

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