Variant report

Variant	rs9467250
Chromosome Location	chr6:24656383-24656384
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:24652620..24654640-chr6:24655230..24656838,2	K562	blood:
2	chr6:24645670..24648708-chr6:24654981..24659486,5	MCF-7	breast:
3	chr6:24653409..24658053-chr6:24717441..24721188,4	MCF-7	breast:
4	chr6:24653780..24658008-chr6:24658421..24664116,7	MCF-7	breast:
5	chr6:24652247..24658784-chr6:24665384..24668018,7	MCF-7	breast:
6	chr6:24653989..24657091-chr6:24719747..24721924,3	MCF-7	breast:
7	chr6:24650977..24653487-chr6:24654406..24656645,3	MCF-7	breast:
8	chr6:24654228..24658025-chr6:24716632..24719423,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000112308	Chromatin interaction
ENSG00000112304	Chromatin interaction
ENSG00000137261	Chromatin interaction
ENSG00000111802	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10085192	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946726	1.00[JPT][hapmap]
rs12393	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs16889581	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];1.00[ASN][1000 genomes]
rs17243493	1.00[EUR][1000 genomes]
rs17243499	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17243513	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17249855	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17249952	1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2493334	1.00[JPT][hapmap]
rs2754771	1.00[JPT][hapmap]
rs2817741	1.00[JPT][hapmap]
rs2817743	1.00[JPT][hapmap]
rs6907640	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6911150	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920675	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6934711	1.00[JPT][hapmap]
rs7743901	1.00[JPT][hapmap]
rs7763865	1.00[JPT][hapmap]
rs9295629	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9461051	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.87[ASN][1000 genomes]
rs9467261	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9467263	0.87[ASN][1000 genomes]
rs9467265	1.00[JPT][hapmap];0.89[YRI][hapmap];0.87[ASN][1000 genomes]
rs9467266	1.00[JPT][hapmap];0.86[YRI][hapmap]
rs9467267	1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3508002	chr6:24618580-24732946	Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	esv3508003	chr6:24618580-24732946	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	nsv601164	chr6:24625091-24661599	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
4	nsv601165	chr6:24632642-24666007	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
5	nsv883481	chr6:24652247-24659071	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24646400-24658800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:24646800-24662400	Weak transcription	Right Ventricle	heart
3	chr6:24646800-24662600	Weak transcription	Spleen	Spleen
4	chr6:24646800-24666000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:24647000-24659000	Weak transcription	Stomach Mucosa	stomach
6	chr6:24647000-24662200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:24647000-24662400	Weak transcription	Lung	lung
8	chr6:24647000-24662600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr6:24647000-24666400	Weak transcription	Esophagus	oesophagus
10	chr6:24647200-24663400	Weak transcription	Fetal Kidney	kidney
11	chr6:24649400-24656600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:24649400-24659200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:24649400-24659600	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr6:24649400-24664800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:24649400-24665200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr6:24650000-24657400	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr6:24650000-24657400	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr6:24650000-24658400	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr6:24650000-24658400	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr6:24650000-24658600	Strong transcription	Rectal Mucosa Donor 29	rectum
21	chr6:24650000-24659000	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr6:24650000-24663600	Strong transcription	Dnd41	blood
23	chr6:24650000-24665000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:24650200-24656600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr6:24650200-24657600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:24650200-24657600	Strong transcription	Placenta	Placenta
27	chr6:24650200-24658800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:24650200-24659000	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr6:24650200-24659000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr6:24650200-24659000	Strong transcription	Duodenum Mucosa	Duodenum
31	chr6:24650400-24658600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr6:24650600-24658800	Strong transcription	H1 Cell Line	embryonic stem cell
33	chr6:24651000-24659800	Strong transcription	Primary B cells from peripheral blood	blood
34	chr6:24651200-24659200	Weak transcription	Small Intestine	intestine
35	chr6:24651400-24656400	Strong transcription	A549	lung
36	chr6:24652400-24662800	Weak transcription	Psoas Muscle	Psoas
37	chr6:24653200-24659000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr6:24653400-24658800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr6:24653400-24662600	Weak transcription	NHLF	lung
40	chr6:24653600-24659200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr6:24653600-24660000	Weak transcription	Rectal Smooth Muscle	rectum
42	chr6:24653800-24658800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr6:24653800-24659000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr6:24653800-24659200	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr6:24653800-24662200	Weak transcription	Fetal Stomach	stomach
46	chr6:24653800-24662200	Weak transcription	Ovary	ovary
47	chr6:24653800-24662400	Weak transcription	Colonic Mucosa	Colon
48	chr6:24653800-24662600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:24653800-24663800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr6:24653800-24666200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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