Variant report

Variant	rs73551676
Chromosome Location	chr11:107373508-107373509
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12098999	0.83[AFR][1000 genomes]
rs12099118	0.90[AFR][1000 genomes]
rs55758825	0.95[AFR][1000 genomes]
rs56345184	0.89[AFR][1000 genomes]
rs59177580	0.90[AFR][1000 genomes]
rs60200073	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61200975	0.86[AFR][1000 genomes]
rs7121279	0.86[AFR][1000 genomes]
rs7122977	0.93[AFR][1000 genomes]
rs73551679	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7928774	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898365	chr11:106944975-107430300	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv898366	chr11:106944975-107433835	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv898367	chr11:106944975-107443420	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv898369	chr11:106958304-107443420	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv898370	chr11:107027991-107430300	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv898372	chr11:107049968-107433835	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1038368	chr11:107116577-107664181	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	nsv541163	chr11:107116577-107664181	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	nsv898373	chr11:107124903-107433835	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	esv2756363	chr11:107189790-107376790	ZNF genes & repeats Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	nsv556376	chr11:107250851-107486598	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv898376	chr11:107299631-107443420	Weak transcription Active TSS Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv533794	chr11:107349817-108093259	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107364000-107394000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr11:107364200-107374000	Weak transcription	NHDF-Ad	bronchial
3	chr11:107364400-107374600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr11:107367200-107375400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr11:107367200-107387400	Weak transcription	Fetal Heart	heart
6	chr11:107367400-107375200	Weak transcription	Brain Angular Gyrus	brain
7	chr11:107369200-107406400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr11:107370000-107433800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr11:107370800-107374800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr11:107371000-107377000	Weak transcription	NHLF	lung
11	chr11:107371000-107383200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:107371200-107374400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr11:107371200-107393000	Weak transcription	Brain Substantia Nigra	brain
14	chr11:107371200-107421200	Weak transcription	Right Ventricle	heart
15	chr11:107371600-107373800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
16	chr11:107372000-107373800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:107372000-107374600	ZNF genes & repeats	Primary T cells from cord blood	blood
18	chr11:107372000-107375800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:107372000-107376600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr11:107372000-107376600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr11:107372000-107376600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr11:107372000-107376600	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr11:107372000-107435600	Weak transcription	Colonic Mucosa	Colon
24	chr11:107372400-107373600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
25	chr11:107372400-107373800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
26	chr11:107372400-107374000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:107372400-107374400	Strong transcription	Skeletal Muscle Female	skeletal muscle
28	chr11:107372400-107376400	Strong transcription	Duodenum Smooth Muscle	Duodenum
29	chr11:107372400-107376600	Strong transcription	Adipose Nuclei	Adipose
30	chr11:107372400-107377000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr11:107372400-107377200	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr11:107372600-107373800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
33	chr11:107372600-107374600	Strong transcription	Colon Smooth Muscle	Colon
34	chr11:107372600-107375400	Strong transcription	Fetal Muscle Leg	muscle
35	chr11:107372600-107375600	Strong transcription	Stomach Smooth Muscle	stomach
36	chr11:107372600-107375800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr11:107372600-107376800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
38	chr11:107372800-107374400	Weak transcription	Fetal Thymus	thymus
39	chr11:107372800-107374800	Weak transcription	Fetal Kidney	kidney
40	chr11:107372800-107375600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr11:107372800-107375600	Weak transcription	Fetal Brain Male	brain
42	chr11:107372800-107389600	Weak transcription	Gastric	stomach
43	chr11:107372800-107409600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr11:107372800-107434600	Weak transcription	Placenta	Placenta
45	chr11:107373000-107373800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr11:107373000-107374400	Weak transcription	HSMM	muscle
47	chr11:107373000-107374400	Weak transcription	HUVEC	blood vessel
48	chr11:107373000-107374800	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr11:107373000-107375000	Weak transcription	Psoas Muscle	Psoas
50	chr11:107373000-107375400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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