Variant report

Variant	rs692191
Chromosome Location	chr19:39622846-39622847
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:39622646..39624803-chr19:39656922..39658959,2	MCF-7	breast:
2	chr19:39615259..39630637-chr19:39640467..39653924,38	MCF-7	breast:
3	chr19:39621056..39623320-chr19:39625823..39628576,3	K562	blood:
4	chr19:39620628..39623686-chr19:39793053..39797178,3	K562	blood:
5	chr19:39622591..39626006-chr19:39627126..39631368,3	MCF-7	breast:
6	chr19:39622616..39624773-chr19:39692455..39694487,2	K562	blood:
7	chr19:39621851..39624607-chr19:39667898..39670113,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269172	Chromatin interaction
ENSG00000130669	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12976130	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12976664	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12977799	0.83[EUR][1000 genomes]
rs1549927	0.88[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs476713	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4803208	1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs490249	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs513053	1.00[ASW][hapmap];0.81[CEU][hapmap];0.86[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs529336	1.00[ASW][hapmap];0.81[CEU][hapmap];0.86[GIH][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs550664	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs554114	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs576527	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs691080	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs691577	1.00[ASW][hapmap];0.81[CEU][hapmap];0.86[GIH][hapmap];1.00[MEX][hapmap];0.80[MKK][hapmap];0.90[TSI][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs692257	0.81[CEU][hapmap];0.82[YRI][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs692337	0.83[CEU][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs692468	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs692475	0.80[CEU][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv458571	chr19:39533754-39628050	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv579508	chr19:39533754-39628050	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1067028	chr19:39567228-39622846	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv1060469	chr19:39567228-39624790	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv833829	chr19:39569681-39730777	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv432048	chr19:39572060-39850060	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs692191	ATP5SL	cis	cerebellum	SCAN
rs692191	PAK4	cis	Thyroid	GTEx

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39617000-39630800	Weak transcription	Primary T cells from cord blood	blood
2	chr19:39617000-39635000	Weak transcription	Aorta	Aorta
3	chr19:39617200-39624800	Enhancers	Left Ventricle	heart
4	chr19:39617400-39659800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr19:39617600-39625600	Enhancers	Spleen	Spleen
6	chr19:39617600-39627600	Enhancers	Fetal Heart	heart
7	chr19:39617800-39623000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr19:39617800-39623200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr19:39617800-39623800	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr19:39617800-39624000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr19:39617800-39624200	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr19:39617800-39624600	Enhancers	Stomach Mucosa	stomach
13	chr19:39617800-39625000	Enhancers	Ovary	ovary
14	chr19:39617800-39625200	Enhancers	Pancreas	Pancrea
15	chr19:39617800-39627200	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr19:39617800-39628600	Enhancers	Placenta	Placenta
17	chr19:39617800-39630200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr19:39617800-39641600	Weak transcription	Thymus	Thymus
19	chr19:39618000-39623600	Enhancers	Brain Angular Gyrus	brain
20	chr19:39618000-39624400	Enhancers	Liver	Liver
21	chr19:39618000-39624600	Enhancers	Fetal Muscle Leg	muscle
22	chr19:39618200-39623600	Genic enhancers	Fetal Intestine Small	intestine
23	chr19:39618200-39623600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr19:39618200-39628400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr19:39618400-39624600	Enhancers	Fetal Muscle Trunk	muscle
26	chr19:39618400-39626800	Weak transcription	NHEK	skin
27	chr19:39618400-39646600	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr19:39619600-39624400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr19:39620000-39623000	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr19:39620000-39627200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr19:39620000-39630000	Weak transcription	HepG2	liver
32	chr19:39620200-39625000	Enhancers	Lung	lung
33	chr19:39620400-39624600	Enhancers	Esophagus	oesophagus
34	chr19:39620400-39624800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr19:39620600-39626800	Enhancers	Fetal Intestine Large	intestine
36	chr19:39621000-39623400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr19:39621000-39623400	Genic enhancers	Fetal Stomach	stomach
38	chr19:39621000-39623600	Enhancers	Adipose Nuclei	Adipose
39	chr19:39621000-39623600	Enhancers	Rectal Smooth Muscle	rectum
40	chr19:39621000-39623600	Enhancers	HUVEC	blood vessel
41	chr19:39621000-39623800	Enhancers	Brain Hippocampus Middle	brain
42	chr19:39621000-39624200	Enhancers	Fetal Kidney	kidney
43	chr19:39621000-39624600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr19:39621000-39624800	Enhancers	Placenta Amnion	Placenta Amnion
45	chr19:39621000-39627200	Enhancers	Fetal Lung	lung
46	chr19:39621000-39628400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr19:39621200-39623000	Enhancers	Primary B cells from peripheral blood	blood
48	chr19:39621200-39623200	Enhancers	Colonic Mucosa	Colon
49	chr19:39621200-39624600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr19:39621400-39623000	Genic enhancers	A549	lung

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