Variant report

Variant	rs61651942
Chromosome Location	chr14:103946998-103946999
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10132290	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10133386	1.00[AMR][1000 genomes]
rs10135716	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10138651	1.00[AMR][1000 genomes]
rs10138842	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10141919	1.00[AMR][1000 genomes]
rs10145990	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10146864	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10147675	1.00[AMR][1000 genomes]
rs10148672	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10151314	1.00[AMR][1000 genomes]
rs11848774	0.96[AFR][1000 genomes]
rs11851727	1.00[AMR][1000 genomes]
rs13379294	1.00[AMR][1000 genomes]
rs13379421	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28631776	1.00[AMR][1000 genomes]
rs35273920	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35586956	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56134485	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56305318	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59330484	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59988848	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60236703	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73353049	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73359944	1.00[AMR][1000 genomes]
rs73359947	1.00[AMR][1000 genomes]
rs8022746	1.00[AMR][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	nsv1049747	chr14:103126148-103955984	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	113 gene(s)	inside rSNPs	diseases
2	nsv534254	chr14:103470073-104023906	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
3	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
4	nsv832883	chr14:103927687-104120953	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
5	nsv525874	chr14:103937372-103950368	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv1829466	chr14:103937582-103954794	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv1835815	chr14:103942991-103989757	Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103922400-103955000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:103923000-103949400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr14:103923200-103976800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:103923600-103967000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr14:103924000-103957400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr14:103925600-103958400	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr14:103926200-103950400	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr14:103926800-103963400	Strong transcription	Fetal Intestine Large	intestine
9	chr14:103927800-103949200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr14:103927800-103951000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
11	chr14:103927800-103951600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr14:103927800-103979800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr14:103928000-103947600	Strong transcription	Fetal Stomach	stomach
14	chr14:103928400-103947600	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr14:103928600-103950800	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr14:103930600-103951800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr14:103931600-103949400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr14:103931600-103955000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr14:103932000-103953800	Strong transcription	Fetal Muscle Leg	muscle
20	chr14:103938000-103949600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr14:103938000-103950200	Weak transcription	Stomach Mucosa	stomach
22	chr14:103939000-103947600	Strong transcription	Left Ventricle	heart
23	chr14:103939200-103949600	Strong transcription	Stomach Smooth Muscle	stomach
24	chr14:103939200-103950800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr14:103939200-103951000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr14:103939200-103951000	Strong transcription	Liver	Liver
27	chr14:103939200-103951000	Strong transcription	Placenta	Placenta
28	chr14:103939200-103966200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr14:103939400-103950400	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr14:103939400-103950800	Strong transcription	Dnd41	blood
31	chr14:103939400-103952200	Strong transcription	Fetal Muscle Trunk	muscle
32	chr14:103939400-103956000	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr14:103939600-103949800	Strong transcription	Osteobl	bone
34	chr14:103940200-103954800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr14:103940400-103948000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr14:103940400-103950400	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr14:103940400-103950800	Strong transcription	Adipose Nuclei	Adipose
38	chr14:103940400-103951000	Strong transcription	Brain Hippocampus Middle	brain
39	chr14:103940600-103947800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr14:103941200-103947200	Strong transcription	Spleen	Spleen
41	chr14:103941200-103949200	Strong transcription	NHEK	skin
42	chr14:103941400-103949200	Strong transcription	Fetal Brain Female	brain
43	chr14:103941600-103949800	Strong transcription	HUVEC	blood vessel
44	chr14:103941600-103953800	Weak transcription	Small Intestine	intestine
45	chr14:103942800-103956000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr14:103942800-103957200	Weak transcription	Brain Angular Gyrus	brain
47	chr14:103942800-103966400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr14:103943200-103947000	Weak transcription	Gastric	stomach
49	chr14:103943200-103969200	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr14:103943400-103948600	Weak transcription	Aorta	Aorta

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