Variant report

Variant	rs71577870
Chromosome Location	chr7:128969178-128969179
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:128968746..128971204-chr7:128973169..128975493,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10235589	0.97[AFR][1000 genomes]
rs10249336	0.89[AFR][1000 genomes]
rs10255583	0.96[AFR][1000 genomes]
rs10269495	0.97[AFR][1000 genomes]
rs10281269	0.91[AFR][1000 genomes]
rs12533108	0.88[AFR][1000 genomes]
rs1405475	0.93[AFR][1000 genomes]
rs1526898	0.89[AFR][1000 genomes]
rs1526899	0.94[AFR][1000 genomes]
rs1549788	0.91[AFR][1000 genomes]
rs1609043	0.93[AFR][1000 genomes]
rs1991645	0.90[AFR][1000 genomes]
rs2402946	0.90[AFR][1000 genomes]
rs2402947	0.91[AFR][1000 genomes]
rs2463096	0.82[AFR][1000 genomes]
rs2566875	0.91[AFR][1000 genomes]
rs2694575	0.94[AFR][1000 genomes]
rs2694583	0.91[AFR][1000 genomes]
rs2694591	0.94[AFR][1000 genomes]
rs2718085	0.91[AFR][1000 genomes]
rs2718090	0.92[AFR][1000 genomes]
rs2718091	0.92[AFR][1000 genomes]
rs2718092	0.82[AFR][1000 genomes]
rs2718097	0.94[AFR][1000 genomes]
rs2718100	0.92[AFR][1000 genomes]
rs28399138	0.89[AFR][1000 genomes]
rs2896414	0.88[AFR][1000 genomes]
rs6467234	0.92[AFR][1000 genomes]
rs6467236	0.93[AFR][1000 genomes]
rs6467239	0.89[AFR][1000 genomes]
rs6949882	0.91[AFR][1000 genomes]
rs6950279	0.91[AFR][1000 genomes]
rs6950496	0.85[AFR][1000 genomes]
rs6970267	0.91[AFR][1000 genomes]
rs71529418	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9641848	0.93[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	nsv525482	chr7:128890812-129045191	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv516498	chr7:128901429-129072024	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	esv3331483	chr7:128918442-129082887	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv428508	chr7:128946738-129114691	Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128956000-128977400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr7:128956200-128971400	Weak transcription	Left Ventricle	heart
3	chr7:128956800-128972400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:128958000-128981000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:128958800-128972000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:128960400-128973200	Weak transcription	Small Intestine	intestine
7	chr7:128963600-128972600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr7:128964200-128972400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:128964200-128981000	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr7:128964400-128976200	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr7:128964600-128981000	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr7:128964800-128976400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr7:128965200-128984200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr7:128965400-128974200	Weak transcription	Primary T cells from cord blood	blood
15	chr7:128965400-128994600	Weak transcription	Primary B cells from cord blood	blood
16	chr7:128965600-128969600	Weak transcription	Fetal Stomach	stomach
17	chr7:128965600-128978200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:128965800-128972600	Weak transcription	Psoas Muscle	Psoas
19	chr7:128965800-128980800	Weak transcription	Fetal Intestine Small	intestine
20	chr7:128965800-128995800	Weak transcription	Primary hematopoietic stem cells	blood
21	chr7:128967000-128972400	Weak transcription	Brain Anterior Caudate	brain
22	chr7:128967200-128971800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:128967200-128972400	Weak transcription	HUVEC	blood vessel
24	chr7:128968200-128972200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr7:128968400-128969200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr7:128969000-128972000	Weak transcription	Muscle Satellite Cultured Cells	--

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