Variant report

Variant	rs59891340
Chromosome Location	chr8:67358795-67358796
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:67358368..67361034-chr8:67361272..67364476,3	K562	blood:
2	chr8:67358722..67361670-chr8:67363913..67366041,2	MCF-7	breast:
3	chr8:67352250..67355147-chr8:67358287..67360742,2	K562	blood:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16932729	1.00[AMR][1000 genomes]
rs57303455	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59180218	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61201861	1.00[AMR][1000 genomes]
rs73691532	1.00[AMR][1000 genomes]
rs73691535	1.00[AMR][1000 genomes]
rs73691541	1.00[AMR][1000 genomes]
rs73691542	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv3414665	chr8:66936816-67381935	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	esv3339106	chr8:67356798-67361196	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67352000-67363600	Weak transcription	Esophagus	oesophagus
2	chr8:67352200-67360200	Weak transcription	Lung	lung
3	chr8:67352200-67360200	Weak transcription	Ovary	ovary
4	chr8:67352200-67360600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:67352200-67361000	Weak transcription	Spleen	Spleen
6	chr8:67352200-67361200	Weak transcription	Gastric	stomach
7	chr8:67352200-67361200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr8:67352200-67364600	Weak transcription	Psoas Muscle	Psoas
9	chr8:67352400-67360200	Weak transcription	Right Ventricle	heart
10	chr8:67352400-67360800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr8:67352400-67361600	Weak transcription	Duodenum Mucosa	Duodenum
12	chr8:67352400-67363600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr8:67352400-67366600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr8:67352600-67363600	Weak transcription	Colon Smooth Muscle	Colon
15	chr8:67353200-67361000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr8:67353200-67361200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr8:67353400-67365400	Weak transcription	Fetal Brain Male	brain
18	chr8:67353400-67368000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:67353600-67360600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr8:67353600-67365200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr8:67353600-67372400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr8:67354000-67360000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:67354000-67367800	Weak transcription	Stomach Mucosa	stomach
24	chr8:67354200-67360400	Weak transcription	Placenta	Placenta
25	chr8:67354800-67359400	Weak transcription	Fetal Intestine Large	intestine
26	chr8:67355000-67361200	Weak transcription	Fetal Intestine Small	intestine
27	chr8:67355000-67365200	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr8:67355400-67361000	Weak transcription	Fetal Stomach	stomach
29	chr8:67355800-67359000	Weak transcription	Fetal Kidney	kidney
30	chr8:67356200-67359400	Strong transcription	Adipose Nuclei	Adipose
31	chr8:67356200-67360600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr8:67356200-67360800	Weak transcription	Fetal Muscle Trunk	muscle
33	chr8:67356200-67362200	Strong transcription	Skeletal Muscle Male	skeletal muscle
34	chr8:67356200-67374400	Strong transcription	Liver	Liver
35	chr8:67356400-67361800	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr8:67356400-67366000	Weak transcription	Fetal Brain Female	brain
37	chr8:67356800-67365600	Strong transcription	Stomach Smooth Muscle	stomach
38	chr8:67357000-67358800	Strong transcription	Aorta	Aorta
39	chr8:67357200-67360800	Weak transcription	Fetal Muscle Leg	muscle
40	chr8:67357400-67359000	Enhancers	Brain Angular Gyrus	brain
41	chr8:67357400-67359000	Enhancers	Brain Substantia Nigra	brain
42	chr8:67357400-67359000	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr8:67357400-67359200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:67357400-67359200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr8:67357400-67359200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:67357400-67359200	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr8:67357400-67365000	Weak transcription	Primary T cells from cord blood	blood
48	chr8:67357600-67358800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr8:67357600-67359000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr8:67357600-67359000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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