Variant report

Variant	rs61843431
Chromosome Location	chr10:43429339-43429340
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:43426456..43429844-chr10:43434614..43436862,3	K562	blood:
2	chr10:43428250..43429844-chr10:43434863..43436862,2	K562	blood:
3	chr10:43428399..43431040-chr10:43431143..43434536,4	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12569973	0.98[ASN][1000 genomes]
rs12572458	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12572459	0.99[ASN][1000 genomes]
rs12572471	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17158301	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17158304	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58477795	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61843422	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61843423	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61843424	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61843425	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61843426	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61843428	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61843430	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61843432	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61843434	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61843435	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61843439	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61843440	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74135422	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74135423	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74135424	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74135429	0.84[EUR][1000 genomes]
rs750328	0.96[ASN][1000 genomes]
rs7899660	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7900242	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7922188	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv550672	chr10:42753190-43441729	Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1042764	chr10:42846383-43511712	Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1050394	chr10:42890663-43604956	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
4	nsv540573	chr10:42890663-43604956	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	nsv534548	chr10:42890664-43729688	Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
6	esv2758216	chr10:42965131-43510191	Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
7	esv2759746	chr10:42965131-43510191	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
8	nsv430159	chr10:43291894-43946294	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh 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

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43427400-43429600	Bivalent Enhancer	Fetal Muscle Leg	muscle
2	chr10:43428000-43429600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
3	chr10:43428000-43429600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
4	chr10:43428000-43429800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr10:43428000-43429800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
6	chr10:43428000-43429800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
7	chr10:43428200-43429400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
8	chr10:43428200-43429600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
9	chr10:43428400-43429400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr10:43428400-43429400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr10:43428400-43429400	Active TSS	Primary T helper naive cells from peripheral blood	blood
12	chr10:43428400-43429400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
13	chr10:43428400-43429400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr10:43428400-43429400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr10:43428400-43429400	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
16	chr10:43428400-43429400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
17	chr10:43428400-43429600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
18	chr10:43428400-43429600	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
19	chr10:43428400-43429600	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
20	chr10:43428400-43429600	Bivalent/Poised TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr10:43428400-43429600	Bivalent Enhancer	Esophagus	oesophagus
22	chr10:43428400-43429600	Bivalent Enhancer	Fetal Brain Male	brain
23	chr10:43428400-43429600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
24	chr10:43428400-43429600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
25	chr10:43428400-43429800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr10:43428400-43429800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
27	chr10:43428400-43429800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
28	chr10:43428400-43429800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr10:43428400-43429800	Bivalent Enhancer	Fetal Stomach	stomach
30	chr10:43428400-43429800	Flanking Active TSS	Fetal Thymus	thymus
31	chr10:43428400-43430000	Enhancers	Gastric	stomach
32	chr10:43428600-43429400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr10:43428600-43429400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
34	chr10:43428600-43429600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
35	chr10:43428600-43429600	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr10:43428600-43429600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr10:43428600-43429600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
38	chr10:43428600-43429600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
39	chr10:43428600-43429600	Bivalent Enhancer	Fetal Lung	lung
40	chr10:43428600-43429600	Bivalent Enhancer	Placenta	Placenta
41	chr10:43428600-43429800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr10:43428600-43429800	Bivalent Enhancer	Left Ventricle	heart
43	chr10:43428600-43429800	Bivalent Enhancer	Lung	lung
44	chr10:43428800-43429400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
45	chr10:43428800-43429400	Bivalent/Poised TSS	HepG2	liver
46	chr10:43428800-43429600	Active TSS	Primary T cells from cord blood	blood
47	chr10:43428800-43429600	Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr10:43428800-43429600	Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr10:43428800-43429600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr10:43428800-43429600	Bivalent Enhancer	Brain Hippocampus Middle	brain

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