Variant report

Variant	rs73172610
Chromosome Location	chr7:100434959-100434960
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:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100395758..100398887-chr7:100432685..100435250,3	K562	blood:
2	chr7:100434732..100436886-chr7:100448043..100451085,4	MCF-7	breast:
3	chr7:100433551..100436484-chr7:100455995..100458424,2	MCF-7	breast:
4	chr7:100269248..100271904-chr7:100434252..100435955,2	MCF-7	breast:
5	chr7:100434387..100436230-chr7:100486746..100488716,2	MCF-7	breast:
6	chr7:100433653..100435265-chr7:100487454..100490757,3	MCF-7	breast:
7	chr7:100433647..100436393-chr7:100462974..100466470,4	MCF-7	breast:
8	chr7:100427087..100431759-chr7:100432300..100436126,8	K562	blood:
9	chr7:100302002..100304028-chr7:100432602..100435007,2	K562	blood:
10	chr7:100428650..100430263-chr7:100434365..100436126,2	K562	blood:
11	chr7:100433315..100435952-chr7:100463569..100466337,4	MCF-7	breast:
12	chr7:100302373..100305778-chr7:100432602..100436293,5	K562	blood:
13	chr7:100434894..100436577-chr7:100440736..100443867,3	K562	blood:
14	chr7:100395163..100402625-chr7:100430790..100439308,9	K562	blood:
15	chr7:100421982..100426777-chr7:100433166..100437776,11	MCF-7	breast:
16	chr7:100182494..100184501-chr7:100433559..100435165,2	K562	blood:
17	chr7:100302203..100304565-chr7:100433455..100435641,2	MCF-7	breast:
18	chr7:100433568..100436428-chr7:100463432..100465884,2	K562	blood:
19	chr7:100025953..100027700-chr7:100433744..100436385,2	K562	blood:
20	chr7:100432969..100436551-chr7:100449855..100451873,3	MCF-7	breast:
21	chr7:100410309..100412230-chr7:100433856..100436732,2	MCF-7	breast:
22	chr7:100427050..100428595-chr7:100433038..100435319,2	MCF-7	breast:
23	chr7:100399758..100401974-chr7:100433436..100436499,4	MCF-7	breast:
24	chr7:100433561..100436547-chr7:100492248..100493882,2	K562	blood:
25	chr7:100433319..100435177-chr7:100470244..100472636,2	MCF-7	breast:
26	chr7:100434202..100436782-chr7:100443711..100446643,3	MCF-7	breast:
27	chr7:100424956..100426805-chr7:100433115..100435139,3	K562	blood:
28	chr7:100415072..100417547-chr7:100433376..100435074,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000172336	Chromatin interaction
ENSG00000087085	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000172354	Chromatin interaction
ENSG00000146828	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000196411	Chromatin interaction
ENSG00000087077	Chromatin interaction
ENSG00000106336	Chromatin interaction
ENSG00000236305	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000176125	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs191137	0.85[EUR][1000 genomes]
rs28373056	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs314303	0.83[EUR][1000 genomes]
rs314308	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs314333	0.83[EUR][1000 genomes]
rs3847060	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3847061	0.92[EUR][1000 genomes]
rs3847062	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41280995	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41280998	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55982265	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56135824	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56173078	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56326327	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59735023	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60720150	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73170798	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73170800	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73172604	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73172605	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	esv1832517	chr7:100355490-100749246	Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758125	chr7:100355490-100749246	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2759547	chr7:100355490-100749246	Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv464647	chr7:100374087-100497131	Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
7	nsv607965	chr7:100374087-100497131	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
8	nsv1032673	chr7:100382250-100606794	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
9	nsv888797	chr7:100386900-100482026	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
10	nsv888798	chr7:100406144-100472826	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
11	nsv888799	chr7:100406144-100497131	Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
12	nsv888800	chr7:100411278-100436446	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
13	nsv888801	chr7:100416250-100497131	Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
14	nsv464648	chr7:100422156-100518458	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
15	nsv607966	chr7:100422156-100518458	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
16	nsv831073	chr7:100425659-100544888	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 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	chr7:100433400-100435200	Enhancers	Gastric	stomach
2	chr7:100433400-100435400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:100433600-100435200	Active TSS	Rectal Smooth Muscle	rectum
4	chr7:100433600-100435400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:100433800-100435200	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr7:100433800-100435200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:100433800-100435400	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr7:100433800-100435400	Active TSS	H9 Cell Line	embryonic stem cell
9	chr7:100433800-100435400	Enhancers	Spleen	Spleen
10	chr7:100434000-100435000	Flanking Active TSS	NHEK	skin
11	chr7:100434000-100435200	Active TSS	H1 Cell Line	embryonic stem cell
12	chr7:100434000-100435200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr7:100434000-100435400	Active TSS	HUES64 Cell Line	embryonic stem cell
14	chr7:100434200-100435000	Flanking Active TSS	Fetal Intestine Large	intestine
15	chr7:100434200-100435000	Flanking Active TSS	Fetal Intestine Small	intestine
16	chr7:100434200-100435000	Flanking Active TSS	Placenta	Placenta
17	chr7:100434200-100435200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:100434200-100435200	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr7:100434200-100435200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:100434200-100435200	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr7:100434200-100435400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:100434200-100435400	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr7:100434200-100435400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr7:100434200-100435400	Active TSS	Duodenum Smooth Muscle	Duodenum
25	chr7:100434400-100435000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:100434400-100435000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:100434400-100435000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr7:100434400-100435200	Active TSS	Colonic Mucosa	Colon
29	chr7:100434400-100435400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
30	chr7:100434600-100435000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:100434600-100435000	Flanking Active TSS	Primary T cells from cord blood	blood
32	chr7:100434600-100435000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:100434600-100435000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
34	chr7:100434600-100435000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr7:100434600-100435000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
36	chr7:100434600-100435000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
37	chr7:100434600-100435000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr7:100434600-100435000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr7:100434600-100435000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr7:100434600-100435000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr7:100434600-100435000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr7:100434600-100435000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:100434600-100435000	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr7:100434600-100435000	Flanking Active TSS	Brain Cingulate Gyrus	brain
45	chr7:100434600-100435000	Flanking Active TSS	Colon Smooth Muscle	Colon
46	chr7:100434600-100435000	Flanking Active TSS	Fetal Brain Male	brain
47	chr7:100434600-100435000	Flanking Active TSS	Fetal Heart	heart
48	chr7:100434600-100435000	Flanking Active TSS	Fetal Lung	lung
49	chr7:100434600-100435000	Flanking Active TSS	Fetal Stomach	stomach
50	chr7:100434600-100435000	Flanking Active TSS	Fetal Thymus	thymus

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