Variant report

Variant	rs7587549
Chromosome Location	chr2:179154663-179154664
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	chr2:179152853..179155708-chr2:179159805..179161811,2	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10203420	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11680778	0.82[CEU][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11692144	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12469658	0.84[EUR][1000 genomes]
rs12473780	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12476671	0.80[EUR][1000 genomes]
rs12693158	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12693160	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13024959	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13382421	0.82[CEU][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13400738	0.82[CEU][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13407992	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1434080	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1865325	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs333992	0.83[JPT][hapmap]
rs333993	0.83[JPT][hapmap]
rs333995	0.82[JPT][hapmap]
rs334604	0.83[JPT][hapmap]
rs334616	0.89[JPT][hapmap]
rs334620	0.86[CEU][hapmap];0.94[JPT][hapmap];0.80[EUR][1000 genomes]
rs334622	0.86[CEU][hapmap];0.94[JPT][hapmap];0.80[EUR][1000 genomes]
rs334623	0.94[JPT][hapmap]
rs334630	1.00[JPT][hapmap]
rs6716156	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6756651	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7599683	0.86[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs9288016	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9288017	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9989738	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009312	chr2:178924318-179215566	Weak transcription Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv536057	chr2:178924318-179215566	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv875452	chr2:178963445-179167766	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1011423	chr2:179084407-179166160	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv834466	chr2:179140792-179284778	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179143000-179160200	Weak transcription	Fetal Kidney	kidney
2	chr2:179143200-179160800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:179143200-179188600	Weak transcription	Brain Anterior Caudate	brain
4	chr2:179144200-179163800	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr2:179144600-179155000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:179145000-179159200	Weak transcription	Liver	Liver
7	chr2:179147400-179162600	Weak transcription	HMEC	breast
8	chr2:179147400-179163000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:179147400-179163000	Weak transcription	NHEK	skin
10	chr2:179147800-179162800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:179150200-179160800	Weak transcription	Psoas Muscle	Psoas
12	chr2:179150600-179160600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr2:179151600-179160800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr2:179151600-179161200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr2:179151800-179155000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr2:179153200-179157200	Weak transcription	K562	blood
17	chr2:179153200-179157400	Weak transcription	Fetal Intestine Large	intestine
18	chr2:179153200-179160200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:179153200-179160200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr2:179153200-179162800	Weak transcription	HUVEC	blood vessel
21	chr2:179154200-179154800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:179154400-179155600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:179154600-179155000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr2:179154600-179155200	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr2:179154600-179155600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:179154600-179155600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain

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