Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:93331530..93334524-chr11:93337032..93340985,4	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1011008	0.81[ASW][hapmap]
rs10831074	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11020422	0.92[ASN][1000 genomes]
rs11020444	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11020447	1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16919080	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16919088	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17564202	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1939563	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1962041	1.00[CEU][hapmap]
rs1986399	0.85[CEU][hapmap]
rs2155244	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3949089	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs41357749	1.00[CEU][hapmap]
rs4478954	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.94[LWK][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57226582	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61918529	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7108777	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7118456	0.82[EUR][1000 genomes]
rs7128771	0.98[EUR][1000 genomes]
rs7928672	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7932373	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7936273	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 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	chr11:93336600-93337400	Enhancers	H1 Cell Line	embryonic stem cell
2	chr11:93336600-93337400	Enhancers	Spleen	Spleen
3	chr11:93336600-93337400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr11:93336600-93337800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr11:93336600-93337800	Enhancers	Fetal Intestine Small	intestine
6	chr11:93336600-93338000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr11:93336600-93339600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr11:93336800-93337400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr11:93336800-93337600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr11:93336800-93337800	Enhancers	Duodenum Mucosa	Duodenum
11	chr11:93336800-93337800	Enhancers	Fetal Intestine Large	intestine
12	chr11:93337000-93337400	Enhancers	H9 Cell Line	embryonic stem cell
13	chr11:93337000-93337400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr11:93337200-93337400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr11:93337200-93337400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:93337200-93337600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr11:93337200-93337800	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr11:93337200-93338600	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr11:93337200-93339000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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