Variant report

Variant	rs35982959
Chromosome Location	chr11:34304787-34304788
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	chr11:34297526..34299830-chr11:34304007..34305753,2	MCF-7	breast:
2	chr11:34303207..34305928-chr11:34378915..34380855,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000166016	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11821411	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11824012	0.86[EUR][1000 genomes]
rs2611108	0.87[EUR][1000 genomes]
rs61117445	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61327783	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73497312	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7938990	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7949237	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757435	chr11:34220504-34370236	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2759816	chr11:34220504-34370236	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv818809	chr11:34239730-34354076	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	esv2753052	chr11:34247462-34358300	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv897205	chr11:34248229-34507213	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv897206	chr11:34253421-34337564	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv897207	chr11:34253683-34621004	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
8	nsv897208	chr11:34257064-34562247	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34296800-34306200	Weak transcription	Fetal Brain Female	brain
2	chr11:34297000-34305000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:34297000-34305200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr11:34297000-34321000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:34297200-34324200	Weak transcription	Aorta	Aorta
6	chr11:34297600-34312600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr11:34298200-34306400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr11:34298400-34305600	Weak transcription	Pancreas	Pancrea
9	chr11:34300400-34306400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr11:34300600-34305400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:34300600-34305600	Weak transcription	Psoas Muscle	Psoas
12	chr11:34300600-34306400	Weak transcription	Left Ventricle	heart
13	chr11:34300800-34306000	Weak transcription	Fetal Lung	lung
14	chr11:34300800-34306400	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr11:34300800-34310200	Weak transcription	HepG2	liver
16	chr11:34300800-34314000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr11:34301200-34305400	Weak transcription	Liver	Liver
18	chr11:34301800-34306400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr11:34303200-34305400	Weak transcription	Fetal Muscle Leg	muscle
20	chr11:34303200-34305400	Weak transcription	Hela-S3	cervix
21	chr11:34303200-34310200	Weak transcription	Right Ventricle	heart
22	chr11:34303400-34323600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:34303600-34305200	Weak transcription	A549	lung

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