Variant report

Variant	rs7104337
Chromosome Location	chr11:76346048-76346049
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:76345106..76346944-chr11:76348405..76350238,2	K562	blood:
2	chr11:76345088..76347686-chr11:76350787..76353535,2	K562	blood:

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs12271056	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2186678	0.83[ASN][1000 genomes]
rs7126722	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7930682	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7947915	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043912	chr11:76301316-76439095	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1039451	chr11:76301316-76440221	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	esv1810781	chr11:76311021-76464814	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76341600-76346200	Weak transcription	Right Atrium	heart
2	chr11:76341600-76346400	Weak transcription	Lung	lung
3	chr11:76341600-76346400	Weak transcription	Right Ventricle	heart
4	chr11:76341600-76347200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr11:76341600-76353000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:76341800-76346800	Weak transcription	Spleen	Spleen
7	chr11:76342000-76346200	Weak transcription	Colonic Mucosa	Colon
8	chr11:76342000-76346600	Weak transcription	Primary B cells from peripheral blood	blood
9	chr11:76342000-76347000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr11:76342000-76347400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:76342200-76346200	Weak transcription	Placenta	Placenta
12	chr11:76342200-76346800	Weak transcription	Primary B cells from cord blood	blood
13	chr11:76342400-76348400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:76342600-76348000	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr11:76342600-76348000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr11:76342800-76347200	Weak transcription	Adipose Nuclei	Adipose
17	chr11:76343800-76347600	Weak transcription	HUVEC	blood vessel
18	chr11:76345200-76349200	Enhancers	Fetal Muscle Leg	muscle
19	chr11:76345200-76349400	Enhancers	Fetal Stomach	stomach
20	chr11:76346000-76347000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:76346000-76349000	Enhancers	Fetal Muscle Trunk	muscle
22	chr11:76346000-76349600	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr11:76346000-76349800	Enhancers	Left Ventricle	heart
24	chr11:76346000-76350800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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