Variant report

Variant	rs11757970
Chromosome Location	chr6:167157794-167157795
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11752971	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11753453	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11964755	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16899331	0.90[ASN][1000 genomes]
rs16899333	0.90[ASN][1000 genomes]
rs17517640	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60336430	0.82[EUR][1000 genomes]
rs6456112	0.90[ASN][1000 genomes]
rs6456115	0.90[ASN][1000 genomes]
rs67162821	0.93[ASN][1000 genomes]
rs6910826	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73051172	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3490076	chr6:166727901-167306743	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
2	esv3490077	chr6:166727901-167306743	Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	nsv605260	chr6:166984094-167455139	Enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
4	nsv432984	chr6:167018915-167181613	Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv482478	chr6:167071366-167265821	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1019381	chr6:167090236-167558598	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
7	nsv538541	chr6:167090236-167558598	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
8	nsv1022866	chr6:167108740-167345629	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	esv1808159	chr6:167151463-167163093	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv482525	chr6:167151805-167324406	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	esv1792808	chr6:167155187-167164571	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv605261	chr6:167156675-167163207	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167152400-167160800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr6:167153600-167157800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:167153800-167160800	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr6:167154600-167158000	Weak transcription	Pancreas	Pancrea
5	chr6:167155800-167157800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:167155800-167157800	Enhancers	Brain Anterior Caudate	brain
7	chr6:167156000-167157800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:167156000-167158000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr6:167156400-167158200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:167156600-167157800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:167156800-167157800	Enhancers	Rectal Smooth Muscle	rectum
12	chr6:167157000-167158000	Enhancers	Fetal Heart	heart
13	chr6:167157000-167158000	Enhancers	NH-A	brain
14	chr6:167157000-167158200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:167157200-167157800	Bivalent Enhancer	Fetal Stomach	stomach
16	chr6:167157200-167157800	Enhancers	Placenta Amnion	Placenta Amnion
17	chr6:167157200-167157800	Enhancers	HSMM	muscle
18	chr6:167157200-167158000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:167157200-167158000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr6:167157200-167158200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr6:167157200-167158400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:167157400-167159000	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr6:167157400-167160800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr6:167157600-167157800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr6:167157600-167157800	Enhancers	Brain Angular Gyrus	brain
26	chr6:167157600-167158000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:167157600-167158200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr6:167157600-167159400	Weak transcription	HSMMtube	muscle
29	chr6:167157600-167161400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr6:167157600-167163600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:167157600-167164200	Weak transcription	Fetal Kidney	kidney

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