Variant report

Variant	rs6705981
Chromosome Location	chr2:11434641-11434642
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	chr2:11433437..11435472-chr2:11482925..11485031,2	MCF-7	breast:
2	chr2:11432453..11434936-chr2:11435134..11437192,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000134318	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10183373	0.83[AFR][1000 genomes]
rs10201229	0.83[AFR][1000 genomes]
rs10205022	0.83[AFR][1000 genomes]
rs10495580	0.91[AFR][1000 genomes]
rs10495581	1.00[AFR][1000 genomes]
rs12329049	0.91[AFR][1000 genomes]
rs12329273	0.91[AFR][1000 genomes]
rs12329341	0.91[AFR][1000 genomes]
rs13388427	0.83[AFR][1000 genomes]
rs13416047	0.83[AFR][1000 genomes]
rs13420367	0.91[AFR][1000 genomes]
rs13431906	0.91[AFR][1000 genomes]
rs1375853	0.83[AFR][1000 genomes]
rs28441302	0.83[AFR][1000 genomes]
rs4267491	0.83[AFR][1000 genomes]
rs55931955	1.00[AFR][1000 genomes]
rs6748868	1.00[AFR][1000 genomes]
rs7583049	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526038	chr2:11369078-11489531	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS 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	19 gene(s)	inside rSNPs	diseases
2	esv1827245	chr2:11385834-11442583	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
4	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11424600-11436600	Weak transcription	Fetal Kidney	kidney
2	chr2:11424800-11455200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr2:11426000-11435800	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr2:11426000-11438200	Weak transcription	Ovary	ovary
5	chr2:11426000-11442400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:11426000-11444800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:11426200-11443400	Weak transcription	HSMM	muscle
8	chr2:11426400-11441600	Weak transcription	Fetal Intestine Small	intestine
9	chr2:11426600-11435800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:11426600-11442600	Weak transcription	Primary T cells from cord blood	blood
11	chr2:11426600-11446000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:11427200-11435600	Weak transcription	Fetal Intestine Large	intestine
13	chr2:11428800-11444200	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr2:11429000-11439800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr2:11429000-11444800	Weak transcription	Left Ventricle	heart
16	chr2:11431600-11435000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:11433000-11437600	Weak transcription	Fetal Heart	heart
18	chr2:11433200-11442600	Weak transcription	Psoas Muscle	Psoas
19	chr2:11433200-11445600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:11433200-11446200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr2:11433400-11443600	Weak transcription	Adipose Nuclei	Adipose
22	chr2:11433600-11435600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:11433600-11435800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr2:11433600-11436200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:11433600-11436800	Weak transcription	Stomach Mucosa	stomach
26	chr2:11433600-11439000	Weak transcription	Liver	Liver
27	chr2:11433600-11443400	Weak transcription	Colon Smooth Muscle	Colon
28	chr2:11433600-11444600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr2:11433600-11446800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr2:11433600-11448000	Weak transcription	Right Ventricle	heart
31	chr2:11433800-11435600	Weak transcription	K562	blood
32	chr2:11433800-11436200	Weak transcription	A549	lung
33	chr2:11433800-11437600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr2:11433800-11438800	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr2:11434000-11438800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr2:11434000-11443400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr2:11434000-11443400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr2:11434600-11438800	Weak transcription	HepG2	liver

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