Variant report

Variant	rs17637637
Chromosome Location	chr2:205315651-205315652
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:205314742..205317390-chr2:205323844..205326602,2	K562	blood:
2	chr2:205314792..205317401-chr2:205318306..205319999,2	K562	blood:
3	chr2:205269954..205272543-chr2:205315221..205317326,2	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10084416	0.93[ASN][1000 genomes]
rs10490267	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs10932063	0.95[ASN][1000 genomes]
rs1156249	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11690070	0.95[ASN][1000 genomes]
rs12472876	1.00[ASN][1000 genomes]
rs12616166	0.87[ASN][1000 genomes]
rs12990859	0.80[EUR][1000 genomes]
rs13003798	0.83[AMR][1000 genomes]
rs13007075	0.83[AMR][1000 genomes]
rs13010221	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13021097	0.83[AMR][1000 genomes]
rs13024043	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1374708	0.95[ASN][1000 genomes]
rs1374709	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1447488	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1447490	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1447493	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1447495	0.89[ASN][1000 genomes]
rs1550909	1.00[JPT][hapmap]
rs17637778	0.83[AMR][1000 genomes]
rs34157021	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34368384	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34816339	0.83[AMR][1000 genomes]
rs35071164	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35207649	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4675457	0.86[ASN][1000 genomes]
rs71427747	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71427750	0.87[AMR][1000 genomes]
rs71427753	0.83[AMR][1000 genomes]
rs7602656	0.89[ASN][1000 genomes]
rs921163	1.00[JPT][hapmap]
rs959032	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs959033	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv964353	chr2:205303005-205473935	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv34706	chr2:205309211-205348724	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205313600-205316600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:205313600-205316800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:205313800-205316000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:205313800-205317000	Enhancers	Colon Smooth Muscle	Colon
5	chr2:205314000-205320000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr2:205314200-205316600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:205314200-205316800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:205314600-205319800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr2:205314800-205315800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:205315200-205316000	Enhancers	K562	blood
11	chr2:205315400-205315800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr2:205315400-205316400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr2:205315400-205316600	Weak transcription	Fetal Brain Male	brain
14	chr2:205315600-205315800	Enhancers	Fetal Lung	lung
15	chr2:205315600-205316000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr2:205315600-205317400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:205315600-205318400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr2:205315600-205318400	Weak transcription	Brain Substantia Nigra	brain
19	chr2:205315600-205318800	Weak transcription	Brain Anterior Caudate	brain

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