Variant report

Variant	rs61990375
Chromosome Location	chr14:71446172-71446173
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10140218	1.00[ASN][1000 genomes]
rs11844339	1.00[ASN][1000 genomes]
rs17766986	1.00[ASN][1000 genomes]
rs45498105	1.00[ASN][1000 genomes]
rs45517434	1.00[ASN][1000 genomes]
rs4902905	1.00[ASN][1000 genomes]
rs4902908	1.00[ASN][1000 genomes]
rs55903050	1.00[ASN][1000 genomes]
rs61988691	1.00[ASN][1000 genomes]
rs61988692	1.00[ASN][1000 genomes]
rs61988693	1.00[ASN][1000 genomes]
rs61988695	1.00[ASN][1000 genomes]
rs61988719	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988721	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988723	0.81[EUR][1000 genomes]
rs61988726	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988727	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988728	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988729	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988735	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988736	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988737	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988738	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61988740	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61989175	1.00[ASN][1000 genomes]
rs61989177	1.00[ASN][1000 genomes]
rs61989179	1.00[ASN][1000 genomes]
rs61989180	1.00[ASN][1000 genomes]
rs61990382	1.00[ASN][1000 genomes]
rs61990383	1.00[ASN][1000 genomes]
rs61990384	1.00[ASN][1000 genomes]
rs61990385	1.00[ASN][1000 genomes]
rs61990404	1.00[ASN][1000 genomes]
rs61990406	1.00[ASN][1000 genomes]
rs61990407	1.00[ASN][1000 genomes]
rs61990408	1.00[ASN][1000 genomes]
rs61990409	1.00[ASN][1000 genomes]
rs61990410	1.00[ASN][1000 genomes]
rs61990411	1.00[ASN][1000 genomes]
rs61990412	1.00[ASN][1000 genomes]
rs61990414	1.00[ASN][1000 genomes]
rs61990416	1.00[ASN][1000 genomes]
rs61990417	1.00[ASN][1000 genomes]
rs61990418	1.00[ASN][1000 genomes]
rs61990420	1.00[ASN][1000 genomes]
rs61990451	1.00[ASN][1000 genomes]
rs61990452	1.00[ASN][1000 genomes]
rs61990453	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:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71426000-71508800	Weak transcription	Psoas Muscle	Psoas
2	chr14:71428000-71446200	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr14:71432000-71446800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr14:71433200-71455200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr14:71437200-71485600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr14:71438600-71502800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr14:71439200-71454800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr14:71439200-71478000	Weak transcription	Colon Smooth Muscle	Colon
9	chr14:71439400-71446400	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr14:71439600-71502800	Weak transcription	Small Intestine	intestine
11	chr14:71440200-71446400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr14:71441200-71447000	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr14:71442800-71446200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr14:71443400-71446200	Strong transcription	HMEC	breast
15	chr14:71443400-71446400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr14:71443400-71446800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
17	chr14:71443600-71446200	Strong transcription	NH-A	brain
18	chr14:71443600-71446400	Strong transcription	Duodenum Smooth Muscle	Duodenum
19	chr14:71443600-71446400	Strong transcription	HUVEC	blood vessel
20	chr14:71443800-71446200	Strong transcription	Fetal Lung	lung
21	chr14:71444600-71446600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:71444800-71446400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
23	chr14:71445000-71446400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr14:71445000-71449800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr14:71445000-71461800	Weak transcription	A549	lung
26	chr14:71445200-71446200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:71445200-71446400	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr14:71445200-71447000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr14:71445200-71447200	Weak transcription	HSMM	muscle
30	chr14:71445200-71447400	Weak transcription	NHLF	lung
31	chr14:71445200-71453800	Weak transcription	Stomach Mucosa	stomach
32	chr14:71445200-71462400	Weak transcription	Esophagus	oesophagus
33	chr14:71445200-71462400	Weak transcription	Gastric	stomach
34	chr14:71445200-71462400	Weak transcription	Lung	lung
35	chr14:71445200-71470800	Weak transcription	GM12878-XiMat	blood
36	chr14:71445200-71471000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr14:71445200-71496200	Weak transcription	Fetal Brain Male	brain
38	chr14:71445200-71497800	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr14:71445200-71502800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:71445200-71510800	Weak transcription	Colonic Mucosa	Colon
41	chr14:71445400-71446200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr14:71445400-71446600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr14:71445400-71446800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr14:71445400-71446800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr14:71445400-71447400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr14:71445400-71447400	Weak transcription	Fetal Brain Female	brain
47	chr14:71445400-71447400	Weak transcription	Fetal Heart	heart
48	chr14:71445400-71447400	Weak transcription	Rectal Smooth Muscle	rectum
49	chr14:71445400-71447400	Weak transcription	Dnd41	blood
50	chr14:71445400-71447600	Enhancers	Primary T helper naive cells from peripheral blood	blood

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