Variant report

Variant	rs11023859
Chromosome Location	chr11:16193033-16193034
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:16192988..16195969-chr11:16626575..16628656,2	K562	blood:
2	chr11:16191988..16194982-chr11:16195738..16200331,5	K562	blood:
3	chr11:16192356..16194022-chr11:16198076..16200331,2	K562	blood:

Variant related genes	Relation type
ENSG00000110693	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10741688	0.92[CEU][hapmap]
rs10832552	0.94[ASN][1000 genomes]
rs10832555	0.93[CEU][hapmap];0.90[EUR][1000 genomes]
rs10832556	0.88[EUR][1000 genomes]
rs10832557	0.88[EUR][1000 genomes]
rs11023860	0.96[CEU][hapmap];0.92[EUR][1000 genomes]
rs1349984	0.89[EUR][1000 genomes]
rs1349985	0.89[EUR][1000 genomes]
rs1349986	0.92[EUR][1000 genomes]
rs1356647	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs1378305	0.96[CEU][hapmap];0.92[EUR][1000 genomes]
rs1455103	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1455104	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs1455109	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs1455111	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs1455113	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1455114	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1455115	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs1455117	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs1455118	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1914875	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs1949482	0.93[CEU][hapmap];0.88[EUR][1000 genomes]
rs1949483	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs2014828	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2054095	0.88[EUR][1000 genomes]
rs2124202	0.93[CEU][hapmap];0.92[EUR][1000 genomes]
rs2168253	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3903292	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs4545520	0.81[CEU][hapmap]
rs4617548	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs4620684	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6486276	0.89[EUR][1000 genomes]
rs6486277	0.88[EUR][1000 genomes]
rs6486278	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs6486279	0.88[EUR][1000 genomes]
rs7102224	0.88[EUR][1000 genomes]
rs7108091	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs7112473	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs7114017	0.88[EUR][1000 genomes]
rs7118395	0.96[CEU][hapmap];0.92[EUR][1000 genomes]
rs7125634	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7131157	0.83[EUR][1000 genomes]
rs7926424	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs7931734	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs7941496	0.92[CEU][hapmap]
rs7950736	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs9651573	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs978294	0.96[CEU][hapmap];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv553562	chr11:16112180-16220289	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv529731	chr11:16122782-16468170	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv897012	chr11:16189326-16283644	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 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	chr11:16185800-16205600	Weak transcription	Fetal Intestine Large	intestine
2	chr11:16189400-16199200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:16190000-16196400	Weak transcription	Fetal Heart	heart
4	chr11:16190800-16194200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:16190800-16194200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr11:16190800-16194400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr11:16190800-16194600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr11:16191000-16194200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr11:16191000-16194800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr11:16191200-16194200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr11:16191400-16194000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr11:16191400-16194800	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr11:16191800-16199600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr11:16192000-16194800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:16192200-16193600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr11:16192400-16193400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr11:16192400-16193400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr11:16192400-16193400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr11:16192400-16193600	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr11:16192600-16193400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr11:16192600-16193600	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr11:16192800-16193800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:16192800-16194000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr11:16193000-16193400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:16193000-16193600	Weak transcription	Fetal Lung	lung
26	chr11:16193000-16195600	Weak transcription	A549	lung

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