Variant report

Variant	rs72929225
Chromosome Location	chr1:70701932-70701933
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	chr1:70671321..70673336-chr1:70700811..70702610,2	K562	blood:

Variant related genes	Relation type
ENSG00000116754	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs56688715	1.00[AMR][1000 genomes]
rs57627286	1.00[AMR][1000 genomes]
rs57928672	1.00[AMR][1000 genomes]
rs59856193	1.00[AMR][1000 genomes]
rs61084750	1.00[AMR][1000 genomes]
rs61493071	1.00[AMR][1000 genomes]
rs72917819	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72917823	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72921081	1.00[AMR][1000 genomes]
rs72929203	1.00[AMR][1000 genomes]
rs72929206	1.00[AMR][1000 genomes]
rs72929207	1.00[AMR][1000 genomes]
rs72929211	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72929214	1.00[AMR][1000 genomes]
rs72929215	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72929226	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72929228	1.00[AMR][1000 genomes]
rs72929237	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72929241	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72929267	1.00[AMR][1000 genomes]
rs72929272	1.00[AMR][1000 genomes]
rs72929277	1.00[AMR][1000 genomes]
rs72929286	1.00[AMR][1000 genomes]
rs72929299	1.00[AMR][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	esv1798518	chr1:70604106-70723347	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	esv1797140	chr1:70604106-70724622	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv871898	chr1:70681486-70723347	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv1014292	chr1:70689215-70799065	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70688000-70710400	Weak transcription	Aorta	Aorta
2	chr1:70688000-70819200	Weak transcription	Esophagus	oesophagus
3	chr1:70688200-70708200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:70688400-70719400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr1:70688600-70719800	Strong transcription	Fetal Thymus	thymus
6	chr1:70689000-70717800	Strong transcription	H1 Cell Line	embryonic stem cell
7	chr1:70689000-70718200	Strong transcription	Placenta	Placenta
8	chr1:70689200-70718600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
9	chr1:70689400-70719200	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr1:70689600-70719200	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr1:70689600-70719200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr1:70690200-70719800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:70690400-70719800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:70690600-70716000	Weak transcription	Stomach Mucosa	stomach
15	chr1:70690600-70719200	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:70690800-70718200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
17	chr1:70690800-70718600	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr1:70690800-70719200	Strong transcription	Duodenum Mucosa	Duodenum
19	chr1:70691200-70717600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr1:70692200-70718200	Strong transcription	Primary B cells from cord blood	blood
21	chr1:70692200-70719200	Strong transcription	Rectal Mucosa Donor 31	rectum
22	chr1:70692400-70717600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr1:70692600-70717000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr1:70692600-70718600	Strong transcription	NH-A	brain
25	chr1:70692800-70702400	Weak transcription	Small Intestine	intestine
26	chr1:70692800-70717800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr1:70692800-70718000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:70692800-70719000	Strong transcription	NHDF-Ad	bronchial
29	chr1:70692800-70719200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:70693200-70718600	Strong transcription	Osteobl	bone
31	chr1:70693200-70719200	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr1:70693400-70718000	Strong transcription	Hela-S3	cervix
33	chr1:70693400-70719000	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr1:70693600-70709600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:70693600-70714600	Strong transcription	Primary hematopoietic stem cells	blood
36	chr1:70693600-70716800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:70693600-70717600	Strong transcription	HepG2	liver
38	chr1:70693600-70717800	Strong transcription	Primary B cells from peripheral blood	blood
39	chr1:70693600-70718200	Strong transcription	Stomach Smooth Muscle	stomach
40	chr1:70693600-70719200	Strong transcription	HUVEC	blood vessel
41	chr1:70693600-70719400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr1:70693600-70719600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:70693800-70718000	Strong transcription	Primary T helper cells PMA-I stimulated	--
44	chr1:70693800-70718200	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr1:70693800-70718600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr1:70693800-70719200	Strong transcription	Primary T cells from cord blood	blood
47	chr1:70693800-70719200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:70693800-70719400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:70693800-70719600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr1:70693800-70719800	Strong transcription	Muscle Satellite Cultured Cells	--

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