Variant report

Variant	rs11738026
Chromosome Location	chr5:177371587-177371588
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10060376	0.82[AMR][1000 genomes]
rs10464066	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10464113	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10464116	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10794706	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11249783	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11742117	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11742168	0.80[AMR][1000 genomes]
rs12186510	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12187456	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13157329	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13157464	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13157845	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13167295	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13167457	0.83[AMR][1000 genomes]
rs13167631	0.82[ASN][1000 genomes]
rs13190413	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4077204	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4077205	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4246052	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4318803	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4318804	0.80[ASN][1000 genomes]
rs4327608	0.88[ASN][1000 genomes]
rs4428434	0.80[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4958942	0.81[ASN][1000 genomes]
rs4958944	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4958945	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4958946	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4958947	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4958948	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4958980	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4958982	0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4958983	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4958984	0.82[ASN][1000 genomes]
rs4958991	0.80[ASN][1000 genomes]
rs4958992	0.88[ASN][1000 genomes]
rs4958995	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4958997	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4958998	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4958999	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4959000	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4959001	0.80[AMR][1000 genomes]
rs4959002	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4959003	0.81[EUR][1000 genomes]
rs60355061	0.82[AMR][1000 genomes]
rs62397830	0.91[ASN][1000 genomes]
rs62397831	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62397832	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6601187	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6601188	0.84[AFR][1000 genomes]
rs6861547	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6864280	0.83[ASN][1000 genomes]
rs6866295	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6875636	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6880829	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6881018	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6885392	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6896989	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs71591890	0.93[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs71591897	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7703493	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7705931	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7706237	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7706255	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7718261	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7730346	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7733233	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9764398	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9765519	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024444	chr5:176751921-177427715	Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	142 gene(s)	inside rSNPs	diseases
2	esv2752795	chr5:176898619-177488281	Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers 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	78 gene(s)	inside rSNPs	diseases
3	nsv1033211	chr5:177133646-177383386	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1030383	chr5:177310325-177571254	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
5	nsv883184	chr5:177311043-177488281	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv883185	chr5:177357964-177401509	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv521629	chr5:177364884-177396200	Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177366400-177378800	Weak transcription	Fetal Intestine Small	intestine
2	chr5:177368200-177396400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr5:177370600-177371800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr5:177370600-177372000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr5:177370600-177372000	Active TSS	Thymus	Thymus
6	chr5:177370600-177372800	Enhancers	Primary B cells from cord blood	blood
7	chr5:177370800-177371600	Enhancers	Liver	Liver
8	chr5:177370800-177371600	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr5:177370800-177371800	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr5:177370800-177371800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
11	chr5:177370800-177371800	Active TSS	Primary T cells from cord blood	blood
12	chr5:177370800-177371800	Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr5:177370800-177371800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
14	chr5:177370800-177371800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr5:177370800-177371800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr5:177370800-177371800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
17	chr5:177370800-177371800	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr5:177370800-177371800	Active TSS	Colonic Mucosa	Colon
19	chr5:177370800-177371800	Active TSS	Rectal Smooth Muscle	rectum
20	chr5:177370800-177371800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
21	chr5:177370800-177371800	Active TSS	HepG2	liver
22	chr5:177370800-177371800	Active TSS	HUVEC	blood vessel
23	chr5:177370800-177372000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
24	chr5:177370800-177373000	Weak transcription	GM12878-XiMat	blood
25	chr5:177371000-177371600	Active TSS	Primary T cells fromperipheralblood	blood
26	chr5:177371000-177371600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:177371000-177371600	Bivalent/Poised TSS	Dnd41	blood
28	chr5:177371000-177371800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
29	chr5:177371000-177371800	Active TSS	Primary T helper cells fromperipheralblood	blood
30	chr5:177371000-177371800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:177371000-177371800	Active TSS	Esophagus	oesophagus
32	chr5:177371000-177371800	Active TSS	Fetal Thymus	thymus
33	chr5:177371000-177371800	Active TSS	Pancreas	Pancrea
34	chr5:177371000-177372000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
35	chr5:177371000-177381800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:177371000-177393000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr5:177371200-177371600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:177371200-177371600	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr5:177371200-177371600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:177371200-177371600	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr5:177371200-177371800	Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr5:177371200-177371800	Active TSS	Primary B cells from peripheral blood	blood
43	chr5:177371200-177371800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
44	chr5:177371200-177371800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr5:177371200-177371800	Active TSS	Psoas Muscle	Psoas
46	chr5:177371200-177371800	Active TSS	Right Ventricle	heart
47	chr5:177371200-177371800	Active TSS	HSMM	muscle
48	chr5:177371200-177372000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr5:177371200-177372000	Active TSS	Muscle Satellite Cultured Cells	--
50	chr5:177371200-177372000	Active TSS	Osteobl	bone

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