Variant report

Variant	rs10118618
Chromosome Location	chr9:107881188-107881189
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	chr9:107877326..107879899-chr9:107880763..107883128,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC44A1-1	chr9:107881012-107881755	XLOC_007499

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10820786	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10820787	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7020422	0.80[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7023003	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7038361	0.96[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs7851083	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7858499	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7872131	0.80[ASN][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	nsv1046935	chr9:107414720-108028061	Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1045108	chr9:107509553-108188550	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:107877000-107883600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr9:107877800-107888600	Weak transcription	NH-A	brain
3	chr9:107878200-107881400	Enhancers	Brain Germinal Matrix	brain
4	chr9:107878200-107883200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr9:107878400-107881200	Weak transcription	Psoas Muscle	Psoas
6	chr9:107878600-107881200	Weak transcription	Adipose Nuclei	Adipose
7	chr9:107878800-107881200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:107878800-107881200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr9:107878800-107881200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr9:107878800-107881200	Weak transcription	Placenta	Placenta
11	chr9:107879000-107881200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr9:107879000-107881200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr9:107879000-107881200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr9:107879000-107881200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:107879000-107881200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr9:107879000-107881200	Weak transcription	Brain Hippocampus Middle	brain
17	chr9:107879000-107881400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr9:107879000-107881600	Weak transcription	Brain Substantia Nigra	brain
19	chr9:107879000-107884000	Weak transcription	Primary T cells from cord blood	blood
20	chr9:107879000-107884000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr9:107879000-107884200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr9:107879000-107884400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr9:107879200-107884000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr9:107879400-107883800	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr9:107879400-107883800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr9:107879400-107884400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr9:107879600-107884200	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr9:107879800-107881200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr9:107879800-107884200	Weak transcription	Fetal Intestine Large	intestine
30	chr9:107879800-107888200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr9:107880000-107881200	Weak transcription	Brain Cingulate Gyrus	brain
32	chr9:107880000-107881200	Weak transcription	Fetal Muscle Leg	muscle
33	chr9:107880000-107881200	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr9:107880000-107881600	Weak transcription	Fetal Muscle Trunk	muscle
35	chr9:107880000-107882600	Weak transcription	Fetal Intestine Small	intestine
36	chr9:107880000-107884200	Weak transcription	Fetal Brain Male	brain
37	chr9:107880200-107881200	Weak transcription	Fetal Thymus	thymus
38	chr9:107880800-107881800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr9:107880800-107881800	Enhancers	Rectal Smooth Muscle	rectum
40	chr9:107881000-107881400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr9:107881000-107881400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr9:107881000-107881400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr9:107881000-107881600	Enhancers	Brain Angular Gyrus	brain
44	chr9:107881000-107881800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr9:107881000-107881800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr9:107881000-107881800	Enhancers	Stomach Smooth Muscle	stomach
47	chr9:107881000-107882000	Enhancers	Colon Smooth Muscle	Colon

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