Variant report

Variant	rs11688839
Chromosome Location	chr2:172890647-172890648
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:172889595..172892508-chr2:172896420..172898140,2	K562	blood:
2	chr2:172889910..172891414-chr2:172938513..172941287,2	MCF-7	breast:
3	chr2:172885240..172888005-chr2:172889269..172891539,4	MCF-7	breast:
4	chr2:172888478..172891307-chr2:172961439..172963560,3	K562	blood:
5	chr2:172885365..172888930-chr2:172890140..172893959,4	K562	blood:

Variant related genes	Relation type
ENSG00000172878	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11673986	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11681005	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11695630	0.87[CEU][hapmap];0.90[CHB][hapmap]
rs12988345	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12988675	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12989544	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12996935	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13013988	0.87[CEU][hapmap];0.80[YRI][hapmap]
rs17500199	0.80[CEU][hapmap];0.86[JPT][hapmap]
rs1965159	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56041936	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62183803	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62183807	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62183812	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62183813	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7580363	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875410	chr2:172693780-172896587	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv875411	chr2:172693780-172942448	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	esv2830399	chr2:172781830-172952526	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv1012188	chr2:172855923-172928891	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172865600-172897400	Weak transcription	Primary T cells from cord blood	blood
2	chr2:172878600-172898200	Weak transcription	Primary B cells from cord blood	blood
3	chr2:172886800-172892800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:172887000-172893200	Weak transcription	Fetal Heart	heart
5	chr2:172887200-172892600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:172887200-172892600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr2:172887200-172892600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:172887200-172892800	Weak transcription	Brain Germinal Matrix	brain
9	chr2:172887200-172894000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:172887200-172894600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr2:172887200-172896600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr2:172887400-172892600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:172887400-172892600	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr2:172887400-172892800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr2:172887400-172892800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr2:172887400-172892800	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr2:172887400-172902800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr2:172887600-172892400	Weak transcription	HepG2	liver
19	chr2:172887600-172892600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:172887600-172892600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr2:172887600-172892800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr2:172887600-172892800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr2:172888600-172892600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:172888600-172892800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr2:172890000-172892800	Weak transcription	K562	blood

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