Variant report

Variant	rs2077501
Chromosome Location	chr7:107824053-107824054
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:107806656..107809513-chr7:107822092..107824990,2	MCF-7	breast:
2	chr7:107822244..107824154-chr7:107832754..107834609,2	MCF-7	breast:
3	chr7:107613209..107614826-chr7:107822149..107824634,2	K562	blood:
4	chr7:107822612..107825209-chr7:108209547..108212442,2	MCF-7	breast:
5	chr7:107823921..107826218-chr7:108097722..108100120,2	MCF-7	breast:
6	chr7:107823153..107825650-chr7:107848931..107851886,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000128590	Chromatin interaction
ENSG00000135241	Chromatin interaction
ENSG00000177683	Chromatin interaction
ENSG00000091129	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10233338	0.92[AFR][1000 genomes]
rs107588	0.82[AFR][1000 genomes]
rs107589	0.93[AFR][1000 genomes]
rs2079710	0.89[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs2142325	0.92[AFR][1000 genomes]
rs371215	0.92[AFR][1000 genomes]
rs3819740	0.93[AFR][1000 genomes]
rs3819742	0.92[AFR][1000 genomes]
rs3819743	0.90[AFR][1000 genomes]
rs3819744	0.92[AFR][1000 genomes]
rs3819745	0.92[AFR][1000 genomes]
rs385432	0.92[AFR][1000 genomes]
rs393266	0.94[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs401433	0.93[AFR][1000 genomes]
rs414892	0.92[AFR][1000 genomes]
rs417455	0.94[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs427909	0.94[AFR][1000 genomes]
rs433870	0.92[AFR][1000 genomes]
rs439657	0.92[AFR][1000 genomes]
rs4730294	0.94[AFR][1000 genomes]
rs4730295	0.94[AFR][1000 genomes]
rs6943271	0.92[AFR][1000 genomes]
rs6970656	0.94[AFR][1000 genomes]
rs97904	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][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	nsv1033979	chr7:107003734-107877761	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv949344	chr7:107396502-107987085	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv831089	chr7:107687618-107877240	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
5	nsv831090	chr7:107786650-108011196	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
6	nsv888941	chr7:107796150-107863395	ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv1030222	chr7:107809927-107844916	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:107786800-107857800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr7:107787800-107844200	Weak transcription	Brain Germinal Matrix	brain
3	chr7:107791000-107824600	Weak transcription	HUVEC	blood vessel
4	chr7:107814200-107828400	Weak transcription	Fetal Intestine Small	intestine
5	chr7:107814800-107830400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:107815600-107829600	Weak transcription	Brain Substantia Nigra	brain
7	chr7:107817400-107828600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr7:107818200-107851800	Weak transcription	HSMMtube	muscle
9	chr7:107818600-107848400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:107818800-107826400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr7:107819800-107828400	Weak transcription	Brain Anterior Caudate	brain
12	chr7:107820000-107830000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr7:107820600-107867400	Weak transcription	Brain Angular Gyrus	brain
14	chr7:107820800-107824800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:107820800-107824800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr7:107820800-107827600	Weak transcription	Fetal Brain Female	brain
17	chr7:107820800-107830600	Weak transcription	Brain Hippocampus Middle	brain
18	chr7:107820800-107834600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:107820800-107840800	Weak transcription	Placenta	Placenta
20	chr7:107820800-107846800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr7:107820800-107850600	Weak transcription	Fetal Intestine Large	intestine
22	chr7:107820800-107851200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:107821000-107824400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:107821000-107824600	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr7:107821000-107852200	Weak transcription	Fetal Muscle Leg	muscle
26	chr7:107821600-107850400	Weak transcription	Fetal Brain Male	brain
27	chr7:107822000-107834000	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr7:107822400-107829200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:107822400-107829200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr7:107822400-107832200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:107823000-107827600	Weak transcription	Pancreas	Pancrea
32	chr7:107823200-107834400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr7:107823400-107824600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr7:107823400-107829600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr7:107823400-107833800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr7:107823800-107825200	Strong transcription	A549	lung
37	chr7:107824000-107825000	Enhancers	K562	blood

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