Variant report

Variant	rs17241442
Chromosome Location	chr9:117825085-117825086
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10117421	1.00[CHB][hapmap];0.82[AMR][1000 genomes]
rs12336431	0.86[AMR][1000 genomes]
rs12342978	0.86[AMR][1000 genomes]
rs1330361	1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1537011	0.80[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17241078	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17241477	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes]
rs17819299	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17819466	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2001357	1.00[ASN][1000 genomes]
rs2150101	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28393206	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4549855	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56961588	0.86[AMR][1000 genomes]
rs57398199	0.82[AMR][1000 genomes]
rs62578423	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62578424	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62578425	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62578426	0.83[EUR][1000 genomes]
rs62578427	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831696	chr9:117701582-117874150	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv615250	chr9:117768021-118012841	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916912	chr9:117770039-118014140	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117782400-117848200	Weak transcription	Brain Substantia Nigra	brain
2	chr9:117791600-117833200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr9:117800800-117825200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr9:117802200-117848200	Weak transcription	Spleen	Spleen
5	chr9:117803600-117825400	Weak transcription	Fetal Kidney	kidney
6	chr9:117809000-117825400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:117812800-117825800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr9:117812800-117830600	Weak transcription	Fetal Lung	lung
9	chr9:117815200-117825200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr9:117815400-117859200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr9:117816000-117825200	Weak transcription	Esophagus	oesophagus
12	chr9:117817800-117850600	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr9:117819200-117827400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr9:117819400-117825800	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr9:117819800-117848000	Weak transcription	Fetal Intestine Small	intestine
16	chr9:117821400-117840200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr9:117821800-117825200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr9:117821800-117825800	Weak transcription	HSMM	muscle
19	chr9:117822000-117826000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr9:117822200-117825200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr9:117822400-117825200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr9:117822400-117825400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr9:117822400-117854400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr9:117822600-117825200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr9:117822800-117825400	Weak transcription	Fetal Intestine Large	intestine
26	chr9:117822800-117825400	Strong transcription	NHDF-Ad	bronchial
27	chr9:117822800-117825400	Strong transcription	Osteobl	bone
28	chr9:117823000-117825200	Strong transcription	Colon Smooth Muscle	Colon
29	chr9:117823000-117826200	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr9:117823200-117825800	Strong transcription	NH-A	brain
31	chr9:117823200-117828000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr9:117823400-117825200	Weak transcription	NHEK	skin
33	chr9:117823600-117825400	Weak transcription	HMEC	breast
34	chr9:117823600-117826000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr9:117823800-117825400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr9:117823800-117825800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr9:117824000-117825200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr9:117824000-117826000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr9:117824200-117825200	Weak transcription	Aorta	Aorta
40	chr9:117824600-117825200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:117824600-117825200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr9:117824600-117828000	Strong transcription	Fetal Stomach	stomach
43	chr9:117825000-117825200	Genic enhancers	Stomach Smooth Muscle	stomach
44	chr9:117825000-117825400	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr9:117825000-117826000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr9:117825000-117826000	Strong transcription	NHLF	lung
47	chr9:117825000-117827400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr9:117825000-117827400	Strong transcription	Fetal Muscle Leg	muscle
49	chr9:117825000-117827400	Enhancers	Rectal Smooth Muscle	rectum
50	chr9:117825000-117828000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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