Variant report

Variant	rs16957793
Chromosome Location	chr15:43799873-43799874
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:43662206..43664068-chr15:43799780..43802571,2	K562	blood:
2	chr15:43791785..43793850-chr15:43798056..43800431,2	K562	blood:
3	15:43792489-43802874..15:44074989-44078735	K562	blood:
4	chr15:43781846..43787403-chr15:43796763..43800745,6	K562	blood:
5	15:43792489-43802874..15:44001645-44015047	GM12878	blood:
6	chr15:43797925..43800191-chr15:43800913..43803440,3	K562	blood:

Variant related genes	Relation type
ENSG00000166963	Chromatin interaction
ENSG00000242866	Chromatin interaction
ENSG00000140265	Chromatin interaction
ENSG00000067369	Chromatin interaction
ENSG00000137822	Chromatin interaction
ENSG00000238494	Chromatin interaction
ENSG00000166763	Chromatin interaction
ENSG00000268488	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12905772	1.00[YRI][hapmap]
rs16957641	0.91[AFR][1000 genomes]
rs16957736	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs16957833	1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2012688	0.91[AFR][1000 genomes]
rs2244746	1.00[YRI][hapmap]
rs2278857	1.00[YRI][hapmap]
rs34823068	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4296223	1.00[YRI][hapmap]
rs4547312	1.00[YRI][hapmap]
rs45490798	0.91[AFR][1000 genomes]
rs45528539	0.81[AFR][1000 genomes]
rs45583832	0.81[AFR][1000 genomes]
rs7163288	0.82[LWK][hapmap];1.00[YRI][hapmap]

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	nsv534649	chr15:43591116-43851142	Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	esv1846172	chr15:43632138-44116986	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats 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	101 gene(s)	inside rSNPs	diseases
3	esv1846701	chr15:43759774-44116986	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
4	nsv437799	chr15:43784000-43989518	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43786000-43801800	Weak transcription	Primary T cells from cord blood	blood
2	chr15:43786200-43801200	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr15:43786200-43801200	Weak transcription	Ovary	ovary
4	chr15:43786400-43801000	Weak transcription	Dnd41	blood
5	chr15:43789400-43801200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr15:43794200-43802000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr15:43795400-43801800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr15:43796200-43800600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr15:43796600-43802000	Weak transcription	Aorta	Aorta
10	chr15:43796800-43802000	Weak transcription	Fetal Kidney	kidney
11	chr15:43798400-43800200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr15:43798400-43800600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:43798400-43800600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr15:43798400-43801000	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr15:43798400-43801200	Weak transcription	Fetal Thymus	thymus
16	chr15:43798600-43800600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr15:43798600-43800600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr15:43798600-43801600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr15:43798800-43800600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr15:43798800-43800600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr15:43798800-43800600	Weak transcription	Fetal Stomach	stomach
22	chr15:43798800-43800600	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr15:43798800-43800600	Weak transcription	Osteobl	bone
24	chr15:43798800-43800800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr15:43798800-43801000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr15:43798800-43801400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr15:43799000-43800400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr15:43799000-43800600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr15:43799000-43800600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:43799000-43800600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr15:43799000-43800600	Weak transcription	NHDF-Ad	bronchial
32	chr15:43799000-43801000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr15:43799000-43801000	Weak transcription	Fetal Lung	lung
34	chr15:43799200-43800600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr15:43799200-43800600	Weak transcription	Fetal Muscle Leg	muscle
36	chr15:43799200-43800600	Weak transcription	HSMM	muscle
37	chr15:43799200-43800600	Weak transcription	K562	blood
38	chr15:43799200-43800800	Weak transcription	HSMMtube	muscle
39	chr15:43799400-43800600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr15:43799400-43800600	Weak transcription	Fetal Heart	heart
41	chr15:43799400-43800800	Weak transcription	NHLF	lung

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