Variant report

Variant	rs1881736
Chromosome Location	chr10:49574826-49574827
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:49559917..49561809-chr10:49572353..49575219,2	MCF-7	breast:
2	chr10:49574275..49576561-chr10:49624083..49626541,2	K562	blood:
3	chr10:49514674..49516304-chr10:49572941..49576035,3	K562	blood:
4	chr10:49574821..49576525-chr10:49722125..49725054,2	K562	blood:

Variant related genes	Relation type
ENSG00000107643	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs1867576	1.00[AMR][1000 genomes]
rs73296284	1.00[AMR][1000 genomes]
rs7914373	1.00[AMR][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	nsv895366	chr10:49299274-49576454	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv467190	chr10:49402084-49576878	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv550811	chr10:49402084-49576878	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49543000-49576200	Weak transcription	Right Atrium	heart
2	chr10:49566400-49580000	Weak transcription	Colon Smooth Muscle	Colon
3	chr10:49568600-49582000	Weak transcription	Psoas Muscle	Psoas
4	chr10:49568800-49576400	Weak transcription	Ovary	ovary
5	chr10:49572000-49577000	Weak transcription	Fetal Heart	heart
6	chr10:49572200-49575800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr10:49572200-49585600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr10:49573400-49576400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr10:49573400-49578600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr10:49573400-49581800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr10:49573400-49588600	Weak transcription	Primary T cells from cord blood	blood
12	chr10:49573600-49576200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr10:49573600-49576200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr10:49573600-49591200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr10:49574000-49576200	Weak transcription	Fetal Kidney	kidney
16	chr10:49574000-49585600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr10:49574200-49575200	Enhancers	HUVEC	blood vessel
18	chr10:49574200-49589800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr10:49574400-49575200	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr10:49574400-49577400	Weak transcription	NHEK	skin
21	chr10:49574600-49576400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr10:49574600-49579800	Weak transcription	Fetal Lung	lung
23	chr10:49574600-49589800	Weak transcription	Primary hematopoietic stem cells	blood
24	chr10:49574600-49589800	Weak transcription	Left Ventricle	heart
25	chr10:49574800-49589800	Weak transcription	A549	lung

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