Variant report

Variant	rs742100
Chromosome Location	chr6:15489578-15489579
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	chr6:15474184..15476635-chr6:15488076..15490844,2	K562	blood:
2	chr6:15243868..15248249-chr6:15486712..15491085,4	K562	blood:

Variant related genes	Relation type
ENSG00000271888	Chromatin interaction
ENSG00000008083	Chromatin interaction

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

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

rs_ID	r²[population]
rs10949304	0.90[ASN][1000 genomes]
rs11964846	0.95[CEU][hapmap];0.94[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11966626	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13192234	0.87[ASW][hapmap];0.95[CEU][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.89[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13192892	0.95[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13194650	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13196869	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13198780	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13202100	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs13202955	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs13204842	1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13208563	0.95[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13209668	0.95[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17455404	0.95[CEU][hapmap];0.85[GIH][hapmap];0.97[TSI][hapmap];0.89[EUR][1000 genomes]
rs1967664	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2076056	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2237138	0.89[EUR][1000 genomes]
rs2299043	0.95[CEU][hapmap];0.95[GIH][hapmap];0.81[MKK][hapmap];0.97[TSI][hapmap];0.86[EUR][1000 genomes]
rs35868206	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3819396	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.89[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.80[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4712251	0.95[CEU][hapmap];0.95[GIH][hapmap];0.89[MEX][hapmap];0.97[TSI][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4715975	0.93[CEU][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4715979	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4715980	0.95[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap];0.95[TSI][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6899342	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6899343	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6917591	0.95[CEU][hapmap];0.88[CHB][hapmap];0.86[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.95[TSI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs742099	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7756331	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7761778	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7769291	1.00[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.89[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7774429	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9383056	0.87[EUR][1000 genomes]
rs9383062	0.94[EUR][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	nsv538140	chr6:15217899-15547127	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv538141	chr6:15234675-15509163	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15461600-15491000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:15471000-15502000	Weak transcription	A549	lung
3	chr6:15480400-15490600	Weak transcription	NHDF-Ad	bronchial
4	chr6:15481200-15491800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:15482200-15491400	Weak transcription	Fetal Brain Male	brain
6	chr6:15482400-15491400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr6:15483200-15490800	Weak transcription	HSMMtube	muscle
8	chr6:15483200-15491400	Weak transcription	Fetal Heart	heart
9	chr6:15484800-15496400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:15486000-15489800	Strong transcription	Primary B cells from peripheral blood	blood
11	chr6:15486200-15489600	Strong transcription	Primary T cells from cord blood	blood
12	chr6:15486200-15491000	Strong transcription	Primary B cells from cord blood	blood
13	chr6:15486200-15491400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:15486400-15490200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:15486400-15491600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr6:15486600-15489800	Strong transcription	GM12878-XiMat	blood
17	chr6:15486600-15490000	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr6:15486600-15490000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
19	chr6:15486600-15490200	Strong transcription	Dnd41	blood
20	chr6:15486600-15491400	Weak transcription	Right Atrium	heart
21	chr6:15486800-15490000	Strong transcription	K562	blood
22	chr6:15486800-15490800	Weak transcription	Psoas Muscle	Psoas
23	chr6:15486800-15502000	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr6:15487000-15489600	Strong transcription	Thymus	Thymus
25	chr6:15487000-15489800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr6:15487000-15490000	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr6:15487000-15490400	Strong transcription	Primary T cells fromperipheralblood	blood
28	chr6:15487000-15490600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr6:15487000-15490800	Strong transcription	Fetal Stomach	stomach
30	chr6:15487200-15489600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:15487200-15489600	Strong transcription	Primary hematopoietic stem cells	blood
32	chr6:15487200-15489800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr6:15487200-15489800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr6:15487200-15489800	Strong transcription	Fetal Intestine Large	intestine
35	chr6:15487200-15489800	Strong transcription	NHEK	skin
36	chr6:15487200-15490200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:15487200-15490200	Genic enhancers	HUES48 Cell Line	embryonic stem cell
38	chr6:15487200-15490200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr6:15487200-15490200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr6:15487200-15490200	Strong transcription	Brain Anterior Caudate	brain
41	chr6:15487200-15490400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:15487200-15491000	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr6:15487200-15508000	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr6:15487400-15489600	Strong transcription	Duodenum Mucosa	Duodenum
45	chr6:15487400-15489800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr6:15487400-15489800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:15487400-15489800	Strong transcription	Fetal Intestine Small	intestine
48	chr6:15487400-15489800	Strong transcription	Fetal Muscle Trunk	muscle
49	chr6:15487400-15489800	Strong transcription	Spleen	Spleen
50	chr6:15487400-15490000	Strong transcription	Adipose Nuclei	Adipose

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