Variant report

Variant	rs61988729
Chromosome Location	chr14:71408043-71408044
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10140218	1.00[ASN][1000 genomes]
rs17766986	1.00[ASN][1000 genomes]
rs45498105	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs45517434	1.00[ASN][1000 genomes]
rs55903050	1.00[ASN][1000 genomes]
rs61988691	1.00[ASN][1000 genomes]
rs61988692	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988693	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988695	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988719	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988721	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988723	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61988726	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988727	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988728	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988735	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988736	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988737	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988738	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988740	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990375	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990382	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990383	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990384	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990385	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990404	1.00[ASN][1000 genomes]
rs61990406	1.00[ASN][1000 genomes]
rs61990407	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990408	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990409	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990410	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990411	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990412	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990414	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990416	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990417	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990418	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990420	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990451	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990452	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990453	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61990458	1.00[ASN][1000 genomes]
rs61992061	1.00[ASN][1000 genomes]
rs61992066	1.00[ASN][1000 genomes]
rs61992068	1.00[ASN][1000 genomes]
rs61992069	1.00[ASN][1000 genomes]
rs61992070	1.00[ASN][1000 genomes]
rs61992080	1.00[ASN][1000 genomes]
rs61992081	1.00[ASN][1000 genomes]
rs61992086	1.00[ASN][1000 genomes]
rs61992088	1.00[ASN][1000 genomes]
rs61992090	1.00[ASN][1000 genomes]
rs61992091	1.00[ASN][1000 genomes]
rs73289980	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041980	chr14:71196358-71767339	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv542125	chr14:71196358-71767339	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1035416	chr14:71212882-71623271	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv542126	chr14:71212882-71623271	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv1049741	chr14:71233043-71462509	Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1037839	chr14:71263886-71625114	Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv542127	chr14:71263886-71625114	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv1038007	chr14:71269747-71667680	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
9	nsv1039769	chr14:71310954-71525720	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	nsv542128	chr14:71310954-71525720	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv565043	chr14:71395604-71625112	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71379600-71408200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr14:71379600-71410400	Weak transcription	Aorta	Aorta
3	chr14:71384200-71408400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr14:71387200-71408400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:71388200-71410400	Weak transcription	Thymus	Thymus
6	chr14:71393400-71408800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr14:71393800-71409000	Weak transcription	Primary B cells from cord blood	blood
8	chr14:71398000-71408400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr14:71398200-71408600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr14:71398400-71410400	Weak transcription	HMEC	breast
11	chr14:71398800-71408600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr14:71401000-71408800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr14:71401000-71443800	Weak transcription	Right Ventricle	heart
14	chr14:71401800-71408600	Weak transcription	Dnd41	blood
15	chr14:71402000-71409200	Weak transcription	A549	lung
16	chr14:71402000-71409200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr14:71402200-71408400	Weak transcription	Fetal Thymus	thymus
18	chr14:71402200-71408600	Weak transcription	Ovary	ovary
19	chr14:71402200-71408800	Weak transcription	Primary T cells from cord blood	blood
20	chr14:71402200-71409200	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr14:71402200-71410400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr14:71402200-71410400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr14:71402200-71410400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr14:71402200-71410400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr14:71402200-71410400	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr14:71402200-71410600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr14:71402200-71410600	Weak transcription	Brain Hippocampus Middle	brain
28	chr14:71402200-71410600	Weak transcription	Left Ventricle	heart
29	chr14:71402200-71412400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr14:71402200-71413600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr14:71402200-71413600	Weak transcription	Osteobl	bone
32	chr14:71402200-71442800	Weak transcription	HSMMtube	muscle
33	chr14:71402400-71408400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:71402400-71410600	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr14:71402400-71410600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr14:71402400-71410600	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr14:71402400-71413600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr14:71402400-71413600	Weak transcription	Fetal Kidney	kidney
39	chr14:71402400-71414400	Weak transcription	Colon Smooth Muscle	Colon
40	chr14:71402600-71409200	Weak transcription	GM12878-XiMat	blood
41	chr14:71402600-71410200	Weak transcription	Duodenum Mucosa	Duodenum
42	chr14:71402600-71410600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr14:71402600-71413800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr14:71402800-71408600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr14:71402800-71408800	Weak transcription	Fetal Intestine Large	intestine
46	chr14:71405400-71408600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr14:71406000-71413800	Weak transcription	Stomach Smooth Muscle	stomach
48	chr14:71406600-71408600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr14:71407200-71408600	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr14:71407200-71408800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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