Variant report

Variant	rs11750835
Chromosome Location	chr5:179935916-179935917
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:179934009..179936437-chr5:179937326..179939535,2	K562	blood:
2	chr5:179935454..179937135-chr5:179951603..179954291,2	MCF-7	breast:
3	chr5:179922992..179929395-chr5:179931202..179936163,8	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11249715	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11249724	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11740121	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11740213	0.80[EUR][1000 genomes]
rs11740953	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11741030	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11742350	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11742375	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11744382	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11744428	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11744582	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11745477	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11745688	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11748724	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11748792	0.80[EUR][1000 genomes]
rs11750477	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11949203	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11956078	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11957507	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11960298	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12109328	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12719870	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13156947	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13171609	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13171921	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13174480	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13179742	0.80[EUR][1000 genomes]
rs13187624	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17630549	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17698422	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35076338	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35197594	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35490561	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56005965	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56039468	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60034484	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62405525	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62405531	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62405532	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023914	chr5:179649883-180040672	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv537983	chr5:179649883-180040672	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1030697	chr5:179710469-180686563	ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	184 gene(s)	inside rSNPs	diseases
4	nsv1026417	chr5:179721376-180291360	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
5	nsv1031836	chr5:179742033-180676122	Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
6	nsv537984	chr5:179742033-180676122	Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
7	nsv949199	chr5:179743553-180696889	Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
8	nsv1023537	chr5:179791679-179982822	Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv537985	chr5:179791679-179982822	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	nsv1019519	chr5:179866730-179959408	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv830564	chr5:179867394-180010096	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179923200-179936400	Weak transcription	Fetal Intestine Large	intestine
2	chr5:179923400-179946000	Weak transcription	Primary B cells from peripheral blood	blood
3	chr5:179923600-179942000	Weak transcription	Spleen	Spleen
4	chr5:179923600-179949800	Weak transcription	Gastric	stomach
5	chr5:179923600-179949800	Weak transcription	Psoas Muscle	Psoas
6	chr5:179923600-179957000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr5:179923800-179941200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr5:179924000-179948000	Weak transcription	A549	lung
9	chr5:179924000-179949800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr5:179924200-179949200	Weak transcription	Pancreas	Pancrea
11	chr5:179924200-179949600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr5:179924200-179950000	Weak transcription	Brain Angular Gyrus	brain
13	chr5:179924600-179941600	Weak transcription	Brain Germinal Matrix	brain
14	chr5:179924600-179944800	Weak transcription	Fetal Brain Male	brain
15	chr5:179924600-179944800	Weak transcription	Fetal Lung	lung
16	chr5:179924600-179949800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr5:179924600-179957000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:179925000-179936200	Weak transcription	Fetal Muscle Trunk	muscle
19	chr5:179925600-179943800	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr5:179925600-179945600	Weak transcription	Lung	lung
21	chr5:179925800-179949200	Weak transcription	Left Ventricle	heart
22	chr5:179926000-179947600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr5:179926800-179948600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr5:179927000-179937000	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr5:179927000-179946000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr5:179927000-179947800	Weak transcription	NHEK	skin
27	chr5:179927000-179948000	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr5:179927000-179954400	Weak transcription	Hela-S3	cervix
29	chr5:179927400-179945800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr5:179927400-179948200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr5:179927400-179948200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:179927400-179949200	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr5:179927400-179949200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:179927400-179949600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:179928000-179941600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:179928600-179945800	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr5:179929000-179959200	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr5:179929200-179945800	Weak transcription	Fetal Brain Female	brain
39	chr5:179931400-179946000	Weak transcription	Osteobl	bone
40	chr5:179931600-179942200	Weak transcription	GM12878-XiMat	blood
41	chr5:179931800-179941400	Weak transcription	HepG2	liver
42	chr5:179933600-179941400	Weak transcription	K562	blood
43	chr5:179933800-179950000	Weak transcription	Colon Smooth Muscle	Colon
44	chr5:179933800-179959000	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr5:179934000-179941400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr5:179934200-179937400	Strong transcription	Dnd41	blood
47	chr5:179934200-179941400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr5:179934200-179948400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:179934200-179949600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr5:179934200-179956600	Weak transcription	Rectal Smooth Muscle	rectum

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