Variant report

Variant	rs60687616
Chromosome Location	chr19:18622424-18622425
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:18615807..18618934-chr19:18622122..18624093,3	K562	blood:
2	chr19:18620701..18622769-chr19:18623745..18625540,2	K562	blood:
3	chr19:18547777..18550611-chr19:18620396..18623306,2	K562	blood:
4	chr19:18620896..18622979-chr19:18626184..18627867,2	K562	blood:
5	chr19:18604323..18606106-chr19:18621396..18623588,2	K562	blood:
6	chr19:18620364..18629414-chr19:18629622..18635316,18	MCF-7	breast:
7	chr19:18620674..18622895-chr19:18698590..18700331,2	K562	blood:

Variant related genes	Relation type
ENSG00000105655	Chromatin interaction
ENSG00000006015	Chromatin interaction
ENSG00000105656	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11574806	0.87[EUR][1000 genomes]
rs16982418	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16982427	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16982429	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16982485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2314669	0.87[EUR][1000 genomes]
rs34078075	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs34868531	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs35328461	1.00[EUR][1000 genomes]
rs58410315	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58604797	1.00[EUR][1000 genomes]
rs58723610	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58842178	1.00[EUR][1000 genomes]
rs59511380	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59549953	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61743938	1.00[EUR][1000 genomes]
rs61743954	0.87[EUR][1000 genomes]
rs7247603	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73523072	0.87[EUR][1000 genomes]
rs73523074	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs8101976	1.00[EUR][1000 genomes]
rs8102397	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
5	nsv1060687	chr19:18522527-18643218	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
6	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
7	nsv1061733	chr19:18574940-18679155	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
8	nsv1055794	chr19:18611545-18676933	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
9	nsv911281	chr19:18613917-18758255	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18600400-18630600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr19:18603600-18622600	Enhancers	Psoas Muscle	Psoas
3	chr19:18606800-18625800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr19:18613800-18631000	Weak transcription	Fetal Brain Female	brain
5	chr19:18616800-18625600	Weak transcription	GM12878-XiMat	blood
6	chr19:18617400-18625400	Weak transcription	Brain Germinal Matrix	brain
7	chr19:18618400-18622600	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr19:18618400-18625800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr19:18618400-18625800	Weak transcription	HMEC	breast
10	chr19:18618600-18624000	Weak transcription	NH-A	brain
11	chr19:18618600-18625400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr19:18618800-18623600	Weak transcription	Brain Angular Gyrus	brain
13	chr19:18618800-18624000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr19:18618800-18624000	Weak transcription	NHDF-Ad	bronchial
15	chr19:18618800-18624200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr19:18618800-18624200	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr19:18618800-18624200	Weak transcription	NHLF	lung
18	chr19:18618800-18625400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr19:18618800-18625600	Weak transcription	Aorta	Aorta
20	chr19:18618800-18626000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr19:18618800-18630000	Weak transcription	Primary hematopoietic stem cells	blood
22	chr19:18618800-18630800	Weak transcription	Thymus	Thymus
23	chr19:18618800-18631000	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr19:18619000-18624200	Weak transcription	Osteobl	bone
25	chr19:18619000-18624800	Weak transcription	Fetal Lung	lung
26	chr19:18619000-18625400	Weak transcription	NHEK	skin
27	chr19:18619000-18625800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr19:18619400-18623600	Weak transcription	Primary T cells from cord blood	blood
29	chr19:18619400-18624800	Weak transcription	Esophagus	oesophagus
30	chr19:18619400-18625400	Weak transcription	Stomach Mucosa	stomach
31	chr19:18619600-18623800	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr19:18619600-18624000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr19:18619600-18625400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr19:18619800-18623800	Weak transcription	Fetal Intestine Large	intestine
35	chr19:18619800-18624000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr19:18619800-18625600	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr19:18619800-18625800	Weak transcription	HSMM	muscle
38	chr19:18620000-18623800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr19:18620000-18625400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr19:18620000-18625600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr19:18620200-18622800	Enhancers	Primary T cells fromperipheralblood	blood
42	chr19:18620200-18623400	Weak transcription	Fetal Stomach	stomach
43	chr19:18620200-18625400	Weak transcription	Brain Cingulate Gyrus	brain
44	chr19:18620200-18625400	Weak transcription	Brain Substantia Nigra	brain
45	chr19:18620200-18630600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr19:18620400-18624000	Weak transcription	Brain Anterior Caudate	brain
47	chr19:18620400-18624200	Weak transcription	Colon Smooth Muscle	Colon
48	chr19:18620800-18623600	Weak transcription	Fetal Heart	heart
49	chr19:18620800-18624200	Weak transcription	Primary B cells from cord blood	blood
50	chr19:18620800-18625000	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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