Variant report

Variant	rs2136375
Chromosome Location	chr8:120821264-120821265
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:120808890..120811019-chr8:120820792..120823982,3	K562	blood:

Variant related genes	Relation type
ENSG00000064313	Chromatin interaction

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10086913	0.88[ASN][1000 genomes]
rs10088232	0.83[ASN][1000 genomes]
rs10092747	0.81[ASN][1000 genomes]
rs10096486	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10101278	0.80[ASN][1000 genomes]
rs10108071	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10109513	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10109901	0.82[ASN][1000 genomes]
rs10109951	0.82[ASN][1000 genomes]
rs10110061	0.80[ASN][1000 genomes]
rs10113252	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10113562	0.82[ASN][1000 genomes]
rs1055130	0.93[ASN][1000 genomes]
rs1055131	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1055133	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12155707	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13258336	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13268676	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13272214	0.84[ASN][1000 genomes]
rs1433952	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1509348	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1567358	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1960439	0.82[ASN][1000 genomes]
rs1976575	0.81[ASN][1000 genomes]
rs2164022	0.84[ASN][1000 genomes]
rs2634	0.82[ASN][1000 genomes]
rs28486048	0.85[ASN][1000 genomes]
rs28715681	0.82[ASN][1000 genomes]
rs28756749	0.82[ASN][1000 genomes]
rs34718068	0.82[ASN][1000 genomes]
rs35019302	0.89[ASN][1000 genomes]
rs35103910	0.80[ASN][1000 genomes]
rs35148850	0.90[ASN][1000 genomes]
rs4380974	0.88[ASN][1000 genomes]
rs4870931	0.85[ASN][1000 genomes]
rs4870955	0.82[ASN][1000 genomes]
rs4870956	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4871577	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4871595	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4871597	0.93[ASN][1000 genomes]
rs4871629	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4871634	0.83[ASN][1000 genomes]
rs4871640	0.82[ASN][1000 genomes]
rs4871648	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4871660	0.82[ASN][1000 genomes]
rs6469846	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs67905698	0.80[ASN][1000 genomes]
rs6982522	0.81[ASN][1000 genomes]
rs6987099	0.82[ASN][1000 genomes]
rs6989559	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6989791	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6992109	0.87[ASN][1000 genomes]
rs6996250	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7012857	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7017010	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7017045	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7813438	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7813680	0.86[ASN][1000 genomes]
rs7821501	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7827482	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7829198	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7832755	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7833490	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7833706	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7837589	0.82[ASN][1000 genomes]
rs7839110	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9297605	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][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	nsv534028	chr8:120348940-120906079	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	nsv949368	chr8:120568034-121019872	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1021071	chr8:120589963-120968317	Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
5	nsv465789	chr8:120636850-120994394	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv612111	chr8:120636850-120994394	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv427826	chr8:120642181-120953395	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	esv3481251	chr8:120800778-120823850	Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv3481253	chr8:120800792-120823847	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120744400-120824400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr8:120781200-120829400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:120781600-120844200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr8:120791000-120833200	Weak transcription	Fetal Heart	heart
5	chr8:120800200-120821800	Strong transcription	HUES6 Cell Line	embryonic stem cell
6	chr8:120801800-120830400	Weak transcription	NHEK	skin
7	chr8:120804800-120824200	Weak transcription	Stomach Mucosa	stomach
8	chr8:120805200-120841400	Weak transcription	Gastric	stomach
9	chr8:120805200-120843000	Weak transcription	Psoas Muscle	Psoas
10	chr8:120806600-120836800	Weak transcription	Esophagus	oesophagus
11	chr8:120808000-120830200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr8:120812000-120821800	Strong transcription	Liver	Liver
13	chr8:120812600-120823000	Strong transcription	Adipose Nuclei	Adipose
14	chr8:120812600-120833000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:120812800-120821400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr8:120812800-120822000	Strong transcription	Fetal Muscle Trunk	muscle
17	chr8:120812800-120822600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
18	chr8:120812800-120822800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:120812800-120822800	Strong transcription	HSMM	muscle
20	chr8:120812800-120823000	Strong transcription	Primary T cells from cord blood	blood
21	chr8:120812800-120823200	Strong transcription	Fetal Thymus	thymus
22	chr8:120812800-120826600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr8:120812800-120834200	Strong transcription	HUES48 Cell Line	embryonic stem cell
24	chr8:120812800-120835000	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr8:120812800-120835400	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr8:120812800-120837600	Strong transcription	Primary B cells from peripheral blood	blood
27	chr8:120812800-120842800	Strong transcription	Primary neutrophils fromperipheralblood	blood
28	chr8:120812800-120843600	Strong transcription	Placenta	Placenta
29	chr8:120813200-120822000	Strong transcription	Duodenum Mucosa	Duodenum
30	chr8:120813200-120823000	Strong transcription	Osteobl	bone
31	chr8:120813200-120829600	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr8:120813400-120821800	Strong transcription	Primary T helper cells PMA-I stimulated	--
33	chr8:120813400-120821800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr8:120813400-120822000	Strong transcription	Primary B cells from cord blood	blood
35	chr8:120813400-120822200	Strong transcription	Fetal Muscle Leg	muscle
36	chr8:120813400-120822600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr8:120813400-120822800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:120813400-120823000	Strong transcription	NH-A	brain
39	chr8:120813400-120824400	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr8:120813400-120826200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr8:120813400-120829600	Weak transcription	HSMMtube	muscle
42	chr8:120813400-120835800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr8:120813400-120844200	Weak transcription	Colonic Mucosa	Colon
44	chr8:120813600-120822000	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr8:120813800-120822200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr8:120813800-120835600	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr8:120814000-120828400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr8:120814000-120843600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr8:120814200-120823200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:120814200-120824200	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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