Variant report

Variant	rs7758337
Chromosome Location	chr6:119104760-119104761
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	chr6:119104519..119106736-chr6:119106969..119109771,2	K562	blood:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs17080706	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61744508	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6900809	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6930200	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7743261	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7750025	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7759672	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7762510	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7765016	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7767856	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7767880	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7773684	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020463	chr6:118593028-119146363	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1025403	chr6:118635123-119122551	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1027444	chr6:118687556-119121660	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv538428	chr6:118687556-119121660	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv949321	chr6:118692304-119137658	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv948980	chr6:118772508-119137658	Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv604559	chr6:118786486-119113317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv1020405	chr6:118786586-119241006	ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
9	nsv830788	chr6:119014021-119143652	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1023826	chr6:119026481-119221408	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv886568	chr6:119044453-119132164	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv886569	chr6:119055873-119132164	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119095200-119105800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:119098200-119104800	Weak transcription	Brain Anterior Caudate	brain
3	chr6:119098600-119105000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr6:119098600-119105000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:119098600-119105600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:119098800-119108800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:119099000-119105800	Weak transcription	Pancreas	Pancrea
8	chr6:119101000-119104800	Weak transcription	Fetal Brain Female	brain
9	chr6:119102200-119104800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:119102400-119105200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:119102400-119105800	Weak transcription	Placenta	Placenta
12	chr6:119102800-119105200	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr6:119103200-119105000	Weak transcription	HMEC	breast
14	chr6:119103200-119105600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr6:119103200-119105600	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr6:119103800-119106000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:119104000-119106600	Enhancers	Ovary	ovary
18	chr6:119104000-119107200	Enhancers	Fetal Lung	lung
19	chr6:119104200-119105200	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr6:119104200-119105600	Enhancers	Brain Substantia Nigra	brain
21	chr6:119104200-119105800	Enhancers	Brain Hippocampus Middle	brain
22	chr6:119104200-119105800	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr6:119104200-119106400	Enhancers	Colon Smooth Muscle	Colon
24	chr6:119104200-119106400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr6:119104200-119106800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:119104200-119107000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr6:119104200-119107000	Enhancers	Brain Cingulate Gyrus	brain
28	chr6:119104200-119107000	Enhancers	Fetal Brain Male	brain
29	chr6:119104200-119107000	Enhancers	Fetal Muscle Leg	muscle
30	chr6:119104200-119107200	Enhancers	Fetal Stomach	stomach
31	chr6:119104400-119105200	Weak transcription	Brain Angular Gyrus	brain
32	chr6:119104400-119105200	Weak transcription	Fetal Heart	heart
33	chr6:119104600-119106800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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