Variant report

Variant	rs59222176
Chromosome Location	chr20:25525118-25525119
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:25524006..25525778-chr20:25527051..25529614,2	MCF-7	breast:
2	chr20:25524378..25525990-chr20:25604731..25606396,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000213742	Chromatin interaction
ENSG00000170191	Chromatin interaction

Extended variants
information (count: 137 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:121)

rs_ID	r²[population]
rs1609701	1.00[ASN][1000 genomes]
rs1888038	1.00[ASN][1000 genomes]
rs2039400	1.00[ASN][1000 genomes]
rs2210053	1.00[ASN][1000 genomes]
rs242122	1.00[ASN][1000 genomes]
rs242124	1.00[ASN][1000 genomes]
rs242125	1.00[ASN][1000 genomes]
rs242131	1.00[ASN][1000 genomes]
rs242134	1.00[ASN][1000 genomes]
rs2482907	1.00[ASN][1000 genomes]
rs2482909	1.00[ASN][1000 genomes]
rs2482917	1.00[ASN][1000 genomes]
rs2482929	1.00[ASN][1000 genomes]
rs2482939	1.00[ASN][1000 genomes]
rs2482942	1.00[ASN][1000 genomes]
rs2482945	1.00[ASN][1000 genomes]
rs2500394	1.00[ASN][1000 genomes]
rs2500396	1.00[ASN][1000 genomes]
rs2500407	1.00[ASN][1000 genomes]
rs2500409	1.00[ASN][1000 genomes]
rs2500412	1.00[ASN][1000 genomes]
rs2500414	1.00[ASN][1000 genomes]
rs2500416	1.00[ASN][1000 genomes]
rs2500419	1.00[ASN][1000 genomes]
rs2500444	1.00[ASN][1000 genomes]
rs2500445	1.00[ASN][1000 genomes]
rs2500447	1.00[ASN][1000 genomes]
rs28801689	1.00[ASN][1000 genomes]
rs2892407	1.00[ASN][1000 genomes]
rs2990515	1.00[ASN][1000 genomes]
rs3002703	1.00[ASN][1000 genomes]
rs364722	1.00[ASN][1000 genomes]
rs366060	1.00[ASN][1000 genomes]
rs368636	1.00[ASN][1000 genomes]
rs368748	1.00[ASN][1000 genomes]
rs371447	1.00[ASN][1000 genomes]
rs378534	1.00[ASN][1000 genomes]
rs379538	1.00[ASN][1000 genomes]
rs380021	1.00[ASN][1000 genomes]
rs384336	1.00[ASN][1000 genomes]
rs388007	1.00[ASN][1000 genomes]
rs394798	1.00[ASN][1000 genomes]
rs400916	1.00[ASN][1000 genomes]
rs409873	1.00[ASN][1000 genomes]
rs409888	1.00[ASN][1000 genomes]
rs417446	1.00[ASN][1000 genomes]
rs417662	1.00[ASN][1000 genomes]
rs423248	1.00[ASN][1000 genomes]
rs426143	1.00[ASN][1000 genomes]
rs428801	1.00[ASN][1000 genomes]
rs429120	1.00[ASN][1000 genomes]
rs432403	1.00[ASN][1000 genomes]
rs439642	1.00[ASN][1000 genomes]
rs442728	1.00[ASN][1000 genomes]
rs448212	1.00[ASN][1000 genomes]
rs4815433	1.00[ASN][1000 genomes]
rs4815434	1.00[ASN][1000 genomes]
rs55822316	1.00[ASN][1000 genomes]
rs56165312	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56751491	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57450264	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59122217	1.00[ASN][1000 genomes]
rs6037112	1.00[ASN][1000 genomes]
rs6037113	1.00[ASN][1000 genomes]
rs6037119	1.00[ASN][1000 genomes]
rs6037147	1.00[ASN][1000 genomes]
rs6037155	1.00[ASN][1000 genomes]
rs6037160	1.00[ASN][1000 genomes]
rs6037172	1.00[ASN][1000 genomes]
rs6037177	1.00[ASN][1000 genomes]
rs6037185	1.00[ASN][1000 genomes]
rs6037194	1.00[ASN][1000 genomes]
rs6037197	1.00[ASN][1000 genomes]
rs6037200	1.00[ASN][1000 genomes]
rs6037209	1.00[ASN][1000 genomes]
rs6037213	1.00[ASN][1000 genomes]
rs60483717	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6050591	1.00[ASN][1000 genomes]
rs6050613	1.00[ASN][1000 genomes]
rs6050618	1.00[ASN][1000 genomes]
rs6050627	1.00[ASN][1000 genomes]
rs6050628	1.00[ASN][1000 genomes]
rs6050695	1.00[ASN][1000 genomes]
rs6050711	1.00[ASN][1000 genomes]
rs6050735	1.00[ASN][1000 genomes]
rs6050740	1.00[ASN][1000 genomes]
rs6050752	1.00[ASN][1000 genomes]
rs6050759	1.00[ASN][1000 genomes]
rs6050772	1.00[ASN][1000 genomes]
rs6050776	1.00[ASN][1000 genomes]
rs6050786	1.00[ASN][1000 genomes]
rs6050806	1.00[ASN][1000 genomes]
rs6050831	1.00[ASN][1000 genomes]
rs6050837	1.00[ASN][1000 genomes]
rs6050839	1.00[ASN][1000 genomes]
rs6050852	1.00[ASN][1000 genomes]
rs6050875	1.00[ASN][1000 genomes]
rs6076360	1.00[ASN][1000 genomes]
rs6076365	1.00[ASN][1000 genomes]
rs6083882	1.00[ASN][1000 genomes]
rs6083883	1.00[ASN][1000 genomes]
rs6083887	1.00[ASN][1000 genomes]
rs6115206	1.00[ASN][1000 genomes]
rs6132844	1.00[ASN][1000 genomes]
rs7263728	1.00[ASN][1000 genomes]
rs73904467	1.00[AMR][1000 genomes]
rs73904468	1.00[AMR][1000 genomes]
rs73904472	1.00[AMR][1000 genomes]
rs73904476	1.00[ASN][1000 genomes]
rs73904490	1.00[AMR][1000 genomes]
rs73904496	1.00[AMR][1000 genomes]
rs73904499	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73904659	1.00[AMR][1000 genomes]
rs73907605	1.00[AMR][1000 genomes]
rs73907608	1.00[AMR][1000 genomes]
rs73907612	1.00[ASN][1000 genomes]
rs73907614	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8116049	1.00[ASN][1000 genomes]
rs913790	1.00[ASN][1000 genomes]
rs913791	1.00[ASN][1000 genomes]
rs913793	1.00[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	nsv1067379	chr20:25355484-25593240	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv1060591	chr20:25388781-25628750	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv544223	chr20:25388781-25628750	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1067441	chr20:25397566-25615439	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv912828	chr20:25433015-25595175	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1062452	chr20:25438025-25590278	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv1066066	chr20:25439367-25588016	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv544224	chr20:25439367-25588016	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv912829	chr20:25444242-25595175	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	nsv912830	chr20:25449945-25595175	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv912831	chr20:25449945-25595868	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
12	nsv994976	chr20:25466406-25593286	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	nsv534623	chr20:25466406-25593296	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv1062765	chr20:25466482-25556751	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv544225	chr20:25466482-25556751	Genic enhancers Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
16	esv2762069	chr20:25506582-25619528	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25498200-25532200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr20:25517800-25554600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr20:25518800-25530200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr20:25520000-25532000	Weak transcription	Dnd41	blood
5	chr20:25520200-25529000	Weak transcription	Stomach Mucosa	stomach
6	chr20:25520600-25527400	Weak transcription	Lung	lung
7	chr20:25520600-25528800	Weak transcription	Gastric	stomach
8	chr20:25521000-25530200	Weak transcription	Brain Germinal Matrix	brain
9	chr20:25521200-25529200	Weak transcription	Placenta	Placenta
10	chr20:25521200-25530600	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr20:25521400-25525200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr20:25521400-25525200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr20:25521400-25525200	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr20:25521400-25525200	Weak transcription	Brain Anterior Caudate	brain
15	chr20:25521400-25525200	Weak transcription	Fetal Stomach	stomach
16	chr20:25521400-25525400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr20:25521400-25525800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr20:25521400-25525800	Weak transcription	Brain Hippocampus Middle	brain
19	chr20:25521400-25525800	Enhancers	Osteobl	bone
20	chr20:25521400-25529200	Weak transcription	Ovary	ovary
21	chr20:25521400-25530000	Weak transcription	HSMM	muscle
22	chr20:25521400-25532200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr20:25521400-25534200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr20:25521600-25526000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr20:25521600-25530200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr20:25521600-25565000	Weak transcription	Aorta	Aorta
27	chr20:25521800-25525200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr20:25522000-25525200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr20:25522000-25530000	Weak transcription	Colon Smooth Muscle	Colon
30	chr20:25522400-25526000	Enhancers	NHLF	lung
31	chr20:25522400-25526400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr20:25522800-25528800	Weak transcription	Spleen	Spleen
33	chr20:25523000-25525200	Weak transcription	Fetal Thymus	thymus
34	chr20:25523000-25527400	Weak transcription	Pancreas	Pancrea
35	chr20:25523000-25529000	Weak transcription	Fetal Intestine Large	intestine
36	chr20:25523000-25529000	Weak transcription	Thymus	Thymus
37	chr20:25523000-25529800	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr20:25523200-25525200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr20:25523200-25526400	Weak transcription	Fetal Intestine Small	intestine
40	chr20:25523400-25525800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr20:25523600-25526000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr20:25523800-25528200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr20:25524000-25525200	Genic enhancers	HepG2	liver
44	chr20:25524000-25525800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr20:25524000-25526000	Enhancers	NH-A	brain
46	chr20:25524000-25526200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr20:25524000-25527200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr20:25524000-25527600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr20:25524000-25529200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr20:25524200-25525200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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