Variant report

Variant	rs7146660
Chromosome Location	chr14:105789397-105789398
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105766174..105769085-chr14:105786529..105791325,5	MCF-7	breast:
2	chr14:105778878..105784143-chr14:105784229..105795178,22	MCF-7	breast:
3	chr14:105766214..105767907-chr14:105789142..105791003,2	MCF-7	breast:
4	chr14:105787616..105789525-chr14:105792023..105794890,2	MCF-7	breast:
5	chr14:105780526..105783453-chr14:105786611..105790632,4	K562	blood:
6	chr14:105788060..105791042-chr14:105819860..105821725,2	MCF-7	breast:
7	chr14:105766895..105769453-chr14:105788043..105790752,2	K562	blood:
8	chr14:105779788..105783141-chr14:105787671..105792848,10	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000185024	Chromatin interaction
ENSG00000179364	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10132353	0.81[YRI][hapmap];1.00[EUR][1000 genomes]
rs10148890	0.80[YRI][hapmap]
rs11847153	0.92[YRI][hapmap];1.00[EUR][1000 genomes]
rs11847295	0.82[ASW][hapmap];0.92[MKK][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11847920	0.80[YRI][hapmap]
rs12101178	0.84[YRI][hapmap];1.00[EUR][1000 genomes]
rs57229884	1.00[EUR][1000 genomes]
rs73357391	1.00[EUR][1000 genomes]
rs73357398	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73359035	1.00[EUR][1000 genomes]
rs9671246	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
4	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
6	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
7	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
8	esv2758369	chr14:105513346-105803170	Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
9	esv2760014	chr14:105513346-105803170	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
10	nsv902441	chr14:105602619-105803170	Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
11	nsv902442	chr14:105602619-105803170	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
12	esv1817919	chr14:105605199-105803170	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv530813	chr14:105607701-106453697	Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
14	nsv902466	chr14:105704465-105803170	Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
15	esv29986	chr14:105707292-105803170	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
16	nsv832887	chr14:105717339-105803170	Strong transcription Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
17	nsv832888	chr14:105717339-105803170	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105782200-105794800	Weak transcription	Small Intestine	intestine
2	chr14:105782600-105793000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr14:105782600-105800000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr14:105782600-105807400	Weak transcription	Primary B cells from cord blood	blood
5	chr14:105782800-105790200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr14:105783000-105790000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:105783000-105796000	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr14:105783000-105796600	Weak transcription	Primary B cells from peripheral blood	blood
9	chr14:105783400-105795600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr14:105783600-105794400	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr14:105783600-105794800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr14:105783600-105795600	Weak transcription	Primary T cells from cord blood	blood
13	chr14:105783600-105795800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr14:105783600-105795800	Weak transcription	Thymus	Thymus
15	chr14:105783600-105796000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr14:105783600-105796000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr14:105783600-105796600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr14:105783600-105799800	Weak transcription	Stomach Mucosa	stomach
19	chr14:105783600-105802800	Weak transcription	Fetal Intestine Large	intestine
20	chr14:105784000-105796800	Weak transcription	NHEK	skin
21	chr14:105784000-105821800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr14:105784200-105795400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr14:105784200-105802400	Weak transcription	Dnd41	blood
24	chr14:105784400-105789600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr14:105784400-105789600	Weak transcription	Right Atrium	heart
26	chr14:105784400-105790400	Weak transcription	NHLF	lung
27	chr14:105784400-105790600	Weak transcription	Fetal Brain Male	brain
28	chr14:105784400-105790600	Weak transcription	Fetal Lung	lung
29	chr14:105784400-105791800	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr14:105784400-105794600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr14:105784400-105796200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr14:105784400-105796400	Weak transcription	HMEC	breast
33	chr14:105784400-105796800	Weak transcription	Aorta	Aorta
34	chr14:105784400-105796800	Weak transcription	Duodenum Mucosa	Duodenum
35	chr14:105784400-105799400	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr14:105784600-105789400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr14:105784600-105789400	Weak transcription	Fetal Muscle Trunk	muscle
38	chr14:105784600-105789400	Weak transcription	Rectal Smooth Muscle	rectum
39	chr14:105784600-105789800	Weak transcription	Adipose Nuclei	Adipose
40	chr14:105784600-105789800	Weak transcription	Colonic Mucosa	Colon
41	chr14:105784600-105791800	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr14:105784600-105795200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr14:105784600-105797000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr14:105784800-105789400	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr14:105784800-105795000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr14:105786200-105789600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr14:105787000-105789400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:105788400-105790800	Strong transcription	Fetal Intestine Small	intestine
49	chr14:105788600-105792200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr14:105788800-105791200	Enhancers	Muscle Satellite Cultured Cells	--

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