Variant report

Variant	rs7354835
Chromosome Location	chr1:168590460-168590461
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	chr1:168590276..168592775-chr1:169444079..169445970,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10800360	0.87[ASN][1000 genomes]
rs10800364	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10800365	0.85[ASN][1000 genomes]
rs10918935	0.85[ASN][1000 genomes]
rs10918939	0.93[ASN][1000 genomes]
rs10918940	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10918941	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10918942	0.93[ASN][1000 genomes]
rs10918944	0.93[ASN][1000 genomes]
rs12022781	0.93[ASN][1000 genomes]
rs12046540	0.87[ASN][1000 genomes]
rs12047717	0.93[ASN][1000 genomes]
rs12093734	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12094908	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12567872	0.80[ASN][1000 genomes]
rs1933088	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2419117	0.93[ASN][1000 genomes]
rs61802611	0.90[ASN][1000 genomes]
rs6659983	0.93[ASN][1000 genomes]
rs6675068	0.87[ASN][1000 genomes]
rs6701804	0.93[ASN][1000 genomes]
rs7354866	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7354986	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7355223	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7514487	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7522695	1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7536834	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014626	chr1:168441288-168642731	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv535196	chr1:168441288-168642731	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1011821	chr1:168441488-168642592	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv535197	chr1:168441488-168642592	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1008852	chr1:168449940-168643905	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv535198	chr1:168449940-168643905	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv1007846	chr1:168449940-168687265	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
9	nsv831836	chr1:168538779-168716956	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv3443	chr1:168577582-168622305	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168583800-168590800	Weak transcription	Brain Angular Gyrus	brain
2	chr1:168583800-168590800	Weak transcription	Fetal Intestine Small	intestine
3	chr1:168583800-168592200	Weak transcription	Aorta	Aorta
4	chr1:168584600-168590600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr1:168584600-168592200	Weak transcription	Right Ventricle	heart
6	chr1:168585200-168590600	Weak transcription	Fetal Muscle Leg	muscle
7	chr1:168588400-168592400	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr1:168588800-168592600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr1:168588800-168592800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr1:168589600-168592400	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr1:168589800-168591200	Enhancers	Adipose Nuclei	Adipose
12	chr1:168589800-168591600	Enhancers	Psoas Muscle	Psoas
13	chr1:168589800-168592400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:168589800-168593200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr1:168589800-168593800	Enhancers	Placenta Amnion	Placenta Amnion
16	chr1:168590200-168590800	Enhancers	Fetal Intestine Large	intestine
17	chr1:168590200-168591000	Enhancers	Right Atrium	heart
18	chr1:168590200-168591200	Enhancers	NH-A	brain
19	chr1:168590400-168590600	Flanking Active TSS	HSMMtube	muscle
20	chr1:168590400-168591000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:168590400-168591000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:168590400-168591000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr1:168590400-168591000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:168590400-168591000	Enhancers	Osteobl	bone
25	chr1:168590400-168591200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr1:168590400-168591200	Enhancers	Muscle Satellite Cultured Cells	--
27	chr1:168590400-168591200	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr1:168590400-168591200	Enhancers	Fetal Heart	heart
29	chr1:168590400-168591200	Enhancers	HSMM	muscle
30	chr1:168590400-168593000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr1:168590400-168593200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:168590400-168595400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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