Variant report

Variant	rs6862944
Chromosome Location	chr5:112360044-112360045
allele	A/G
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:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:41464794..41468593-chr5:112359198..112362218,8	MCF-7	breast:
2	chr11:62609128..62610653-chr5:112359196..112360717,2	MCF-7	breast:
3	chr11:62607617..62610650-chr5:112359197..112362197,3	K562	blood:
4	chr11:62607653..62610646-chr5:112359197..112360718,4	K562	blood:
5	chr3:73158608..73161441-chr5:112359196..112360716,4	K562	blood:
6	chr17:41464595..41468045-chr5:112359196..112362218,12	K562	blood:
7	chr3:73160015..73162090-chr5:112359196..112360717,2	MCF-7	breast:
8	chr17:41398761..41400393-chr5:112359218..112362196,2	K562	blood:
9	chr17:41464180..41467892-chr5:112359196..112362218,12	K562	blood:
10	chr3:73158611..73160133-chr5:112359196..112360717,3	K562	blood:
11	chr13:90585208..90586708-chr5:112359217..112360718,2	K562	blood:
12	chr17:41391742..41394689-chr5:112359196..112360716,2	K562	blood:
13	chr17:41445379..41447099-chr5:112359216..112362198,2	K562	blood:
14	chr17:41398893..41402334-chr5:112359196..112362218,6	K562	blood:
15	chr18:21285883..21287403-chr5:112359197..112360718,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000133316	Chromatin interaction
ENSG00000223247	Chromatin interaction
ENSG00000188825	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs12108764	1.00[YRI][hapmap]
rs12521395	0.89[AMR][1000 genomes]
rs13185006	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1562017	1.00[YRI][hapmap]
rs17310536	1.00[AMR][1000 genomes]
rs17311019	1.00[AMR][1000 genomes]
rs17311096	1.00[AMR][1000 genomes]
rs17369211	1.00[AMR][1000 genomes]
rs17369487	1.00[AMR][1000 genomes]
rs17370550	0.89[AMR][1000 genomes]
rs4235775	0.84[EUR][1000 genomes]
rs4235776	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4235780	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4235781	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4235782	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4235783	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4235784	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4235785	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4260661	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4276396	0.84[EUR][1000 genomes]
rs4295378	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4374752	1.00[YRI][hapmap]
rs4519915	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4627978	0.84[EUR][1000 genomes]
rs4705534	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4705535	0.89[AMR][1000 genomes]
rs4705536	0.84[EUR][1000 genomes]
rs4705757	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4705759	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4705760	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4705761	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4705764	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4705765	0.84[EUR][1000 genomes]
rs55798475	1.00[AMR][1000 genomes]
rs55901036	1.00[AMR][1000 genomes]
rs55940904	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56023848	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56265422	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs59876839	1.00[AFR][1000 genomes]
rs6594657	1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6594658	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6594664	1.00[CEU][hapmap]
rs6594666	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6594667	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6594668	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6594681	1.00[YRI][hapmap]
rs6872473	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6881198	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6881233	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6881426	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6881477	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6882115	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6895843	1.00[YRI][hapmap]
rs6897972	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7706745	1.00[AMR][1000 genomes]
rs7728495	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs878074	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs878075	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv599394	chr5:112185491-112446323	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv882717	chr5:112336588-112408944	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 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	chr5:112314200-112362600	Weak transcription	Colonic Mucosa	Colon
2	chr5:112315600-112362600	Weak transcription	Brain Angular Gyrus	brain
3	chr5:112317800-112366200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:112318400-112365600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr5:112319800-112363800	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr5:112320000-112364200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:112320600-112362600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:112321200-112364800	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr5:112321400-112363800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr5:112322600-112362400	Weak transcription	Psoas Muscle	Psoas
11	chr5:112322800-112362400	Weak transcription	Esophagus	oesophagus
12	chr5:112324800-112369800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:112327800-112364600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:112330200-112362800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:112332400-112372600	Weak transcription	Fetal Brain Male	brain
16	chr5:112333200-112362400	Weak transcription	Right Ventricle	heart
17	chr5:112334000-112365200	Strong transcription	Placenta	Placenta
18	chr5:112338600-112360800	Weak transcription	Aorta	Aorta
19	chr5:112339200-112362400	Weak transcription	Pancreas	Pancrea
20	chr5:112339400-112362000	Weak transcription	Gastric	stomach
21	chr5:112340400-112362400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr5:112340400-112362600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr5:112340400-112362600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr5:112342200-112362600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr5:112349800-112362400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr5:112349800-112366600	Weak transcription	Colon Smooth Muscle	Colon
27	chr5:112350000-112360600	Weak transcription	Fetal Intestine Small	intestine
28	chr5:112350200-112361400	Weak transcription	Brain Substantia Nigra	brain
29	chr5:112350200-112361400	Weak transcription	Lung	lung
30	chr5:112350200-112361400	Weak transcription	Ovary	ovary
31	chr5:112350200-112362000	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr5:112350200-112362600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:112350200-112362600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr5:112350200-112362600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr5:112350200-112362600	Weak transcription	Brain Anterior Caudate	brain
36	chr5:112350200-112362800	Weak transcription	Brain Cingulate Gyrus	brain
37	chr5:112350400-112360800	Weak transcription	Fetal Intestine Large	intestine
38	chr5:112350400-112361000	Weak transcription	Fetal Stomach	stomach
39	chr5:112350400-112361400	Weak transcription	Stomach Smooth Muscle	stomach
40	chr5:112350400-112361800	Weak transcription	Brain Hippocampus Middle	brain
41	chr5:112350400-112362000	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr5:112350400-112362400	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr5:112350400-112362400	Weak transcription	Spleen	Spleen
44	chr5:112350400-112362600	Weak transcription	Fetal Brain Female	brain
45	chr5:112350400-112362600	Weak transcription	Rectal Smooth Muscle	rectum
46	chr5:112350400-112362600	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr5:112350600-112362400	Weak transcription	Brain Germinal Matrix	brain
48	chr5:112351000-112361800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:112351200-112362600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr5:112352400-112367800	Strong transcription	Liver	Liver

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