Variant report

Variant	rs9467373
Chromosome Location	chr6:24981223-24981224
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:24979064..24981330-chr6:25006890..25009589,2	K562	blood:
2	chr6:24980023..24981971-chr6:24983813..24985349,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs13190691	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35685833	0.88[ASN][1000 genomes]
rs364769	0.90[ASN][1000 genomes]
rs400592	0.90[ASN][1000 genomes]
rs401671	0.88[ASN][1000 genomes]
rs620589	0.87[ASN][1000 genomes]
rs621948	0.83[ASN][1000 genomes]
rs650386	0.83[ASN][1000 genomes]
rs660840	0.90[ASN][1000 genomes]
rs66827126	0.82[ASN][1000 genomes]
rs7773555	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9295642	0.83[ASN][1000 genomes]
rs9467375	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022966	chr6:24763776-25154212	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv538160	chr6:24763776-25154212	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1019504	chr6:24869174-24994758	Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv883482	chr6:24926730-25035920	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv1023989	chr6:24930362-25285679	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS 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	43 gene(s)	inside rSNPs	diseases
6	nsv1030634	chr6:24938277-25040161	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	nsv830610	chr6:24951741-25124239	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24950400-24988600	Weak transcription	Dnd41	blood
2	chr6:24976600-24981600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr6:24977800-24982000	Enhancers	H9 Cell Line	embryonic stem cell
4	chr6:24977800-24982400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:24977800-24986000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr6:24978800-24982000	Enhancers	Primary B cells from peripheral blood	blood
7	chr6:24978800-24989400	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr6:24979000-24983400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr6:24979000-24984200	Enhancers	Placenta Amnion	Placenta Amnion
10	chr6:24979000-24988800	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr6:24979200-24981800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr6:24979200-24983200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr6:24979200-24983200	Enhancers	HSMM	muscle
14	chr6:24979200-24983200	Enhancers	HSMMtube	muscle
15	chr6:24979200-24983400	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr6:24979200-24983600	Enhancers	NHDF-Ad	bronchial
17	chr6:24979200-24983800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr6:24979200-24984400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:24979400-24981800	Enhancers	Fetal Heart	heart
20	chr6:24979400-24982000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr6:24979400-24983000	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr6:24979600-24983400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:24979800-24983800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr6:24980000-24985000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr6:24980000-24986200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr6:24980000-24989200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr6:24980200-24981400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr6:24980200-24983800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:24980200-24990400	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr6:24980400-24983400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:24980600-24982000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr6:24980600-24982000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr6:24980600-24982200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:24980600-24982200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:24980600-24982200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:24980600-24983200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr6:24980600-24983200	Enhancers	Primary T cells from cord blood	blood
38	chr6:24980600-24983400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr6:24980600-24983400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr6:24980800-24981600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr6:24980800-24981800	Enhancers	Gastric	stomach
42	chr6:24980800-24981800	Enhancers	Lung	lung
43	chr6:24980800-24982000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr6:24980800-24982000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr6:24980800-24982200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:24980800-24982200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr6:24980800-24982200	Enhancers	Pancreas	Pancrea
48	chr6:24980800-24982400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:24980800-24982400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr6:24980800-24982400	Enhancers	Primary T cells fromperipheralblood	blood

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