Variant report

Variant	rs73498365
Chromosome Location	chr9:100421308-100421309
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:100402497..100405197-chr9:100418612..100421386,2	MCF-7	breast:
2	chr9:100394763..100397690-chr9:100420038..100423613,3	MCF-7	breast:
3	chr9:100410166..100412202-chr9:100420931..100422531,3	K562	blood:
4	chr9:100420145..100421947-chr9:100439982..100442814,2	K562	blood:
5	chr9:100418467..100422475-chr9:100423692..100426910,4	MCF-7	breast:
6	chr9:100403992..100406987-chr9:100418866..100421676,2	K562	blood:

Variant related genes	Relation type
ENSG00000136937	Chromatin interaction
ENSG00000136925	Chromatin interaction

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs16923033	0.94[AFR][1000 genomes]
rs16923041	0.81[AFR][1000 genomes]
rs16923112	0.86[AFR][1000 genomes]
rs1813875	0.94[AFR][1000 genomes]
rs2297155	0.86[AFR][1000 genomes]
rs2297156	0.86[AFR][1000 genomes]
rs2297158	0.86[AFR][1000 genomes]
rs2297159	0.86[AFR][1000 genomes]
rs2297160	0.86[AFR][1000 genomes]
rs2401635	0.86[AFR][1000 genomes]
rs3176623	0.86[AFR][1000 genomes]
rs3176624	0.86[AFR][1000 genomes]
rs3176626	0.86[AFR][1000 genomes]
rs3176628	0.86[AFR][1000 genomes]
rs3176629	0.86[AFR][1000 genomes]
rs3176634	0.82[AFR][1000 genomes]
rs3176635	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3176637	0.86[AFR][1000 genomes]
rs3176638	0.86[AFR][1000 genomes]
rs3176644	0.86[AFR][1000 genomes]
rs3176651	0.86[AFR][1000 genomes]
rs3176657	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3176659	0.86[AFR][1000 genomes]
rs3176668	0.86[AFR][1000 genomes]
rs3176669	0.86[AFR][1000 genomes]
rs3176670	0.86[AFR][1000 genomes]
rs3176675	0.86[AFR][1000 genomes]
rs3176682	0.86[AFR][1000 genomes]
rs3176685	0.86[AFR][1000 genomes]
rs3176687	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3176688	0.83[AFR][1000 genomes]
rs3176694	0.86[AFR][1000 genomes]
rs3176706	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3176708	0.86[AFR][1000 genomes]
rs3176711	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3176712	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3176714	0.86[AFR][1000 genomes]
rs3176720	0.86[AFR][1000 genomes]
rs3176723	0.86[AFR][1000 genomes]
rs3176724	0.86[AFR][1000 genomes]
rs3176726	0.86[AFR][1000 genomes]
rs3176735	0.86[AFR][1000 genomes]
rs3176736	0.86[AFR][1000 genomes]
rs3176740	0.86[AFR][1000 genomes]
rs3176744	0.85[AFR][1000 genomes]
rs3176746	0.86[AFR][1000 genomes]
rs3176747	0.86[AFR][1000 genomes]
rs56052819	0.86[AFR][1000 genomes]
rs56200116	0.86[AFR][1000 genomes]
rs57598118	0.86[AFR][1000 genomes]
rs59354722	0.86[AFR][1000 genomes]
rs59662386	0.81[AFR][1000 genomes]
rs59775587	0.86[AFR][1000 genomes]
rs60055057	0.81[AFR][1000 genomes]
rs60463150	0.86[AFR][1000 genomes]
rs60821994	0.86[AFR][1000 genomes]
rs61208411	0.86[AFR][1000 genomes]
rs61221847	0.81[AFR][1000 genomes]
rs61440789	0.86[AFR][1000 genomes]
rs61739366	0.91[AFR][1000 genomes]
rs6478305	0.89[AFR][1000 genomes]
rs7021377	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7045160	0.86[AFR][1000 genomes]
rs7341850	0.81[AFR][1000 genomes]
rs73498323	0.93[AFR][1000 genomes]
rs73498329	0.94[AFR][1000 genomes]
rs73498332	0.81[AFR][1000 genomes]
rs73498338	0.81[AFR][1000 genomes]
rs73498347	0.81[AFR][1000 genomes]
rs73498348	0.81[AFR][1000 genomes]
rs73498355	0.81[AFR][1000 genomes]
rs73498358	0.81[AFR][1000 genomes]
rs73498359	0.94[AFR][1000 genomes]
rs73498362	0.81[AFR][1000 genomes]
rs73498377	0.86[AFR][1000 genomes]
rs73498380	0.86[AFR][1000 genomes]
rs73498381	0.86[AFR][1000 genomes]
rs73500307	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73500321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73500325	0.86[AFR][1000 genomes]
rs73500326	0.83[AFR][1000 genomes]
rs73500328	0.86[AFR][1000 genomes]
rs73500392	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73500393	0.86[AFR][1000 genomes]
rs73500395	0.86[AFR][1000 genomes]
rs73500396	0.86[AFR][1000 genomes]
rs73500397	0.86[AFR][1000 genomes]
rs73500398	0.86[AFR][1000 genomes]
rs73500400	0.86[AFR][1000 genomes]
rs73502208	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs73502210	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs73551090	0.91[AFR][1000 genomes]
rs73554650	0.90[AFR][1000 genomes]
rs7850986	0.86[AFR][1000 genomes]
rs7857174	0.90[AFR][1000 genomes]
rs7859979	0.90[AFR][1000 genomes]
rs7862356	0.86[AFR][1000 genomes]
rs7866961	0.81[AFR][1000 genomes]
rs7869683	0.81[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893610	chr9:100324086-100496160	Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 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	chr9:100399200-100421400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:100399600-100426800	Weak transcription	Stomach Mucosa	stomach
3	chr9:100400800-100451600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr9:100401200-100429000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr9:100401200-100456000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr9:100402400-100422400	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr9:100402400-100425000	Strong transcription	Primary B cells from cord blood	blood
8	chr9:100402400-100439600	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr9:100402400-100451400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:100402400-100455600	Strong transcription	Dnd41	blood
11	chr9:100402600-100456000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr9:100402600-100456200	Strong transcription	Primary B cells from peripheral blood	blood
13	chr9:100402800-100429000	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr9:100402800-100454200	Strong transcription	Fetal Thymus	thymus
15	chr9:100402800-100456000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:100403000-100422600	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr9:100403000-100428400	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr9:100403000-100439400	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr9:100403000-100439800	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr9:100403000-100449400	Strong transcription	HSMM	muscle
21	chr9:100403000-100450400	Strong transcription	Duodenum Mucosa	Duodenum
22	chr9:100403000-100454400	Strong transcription	Placenta	Placenta
23	chr9:100403000-100454600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr9:100403200-100454400	Strong transcription	Rectal Mucosa Donor 31	rectum
25	chr9:100403200-100455000	Strong transcription	Primary T cells fromperipheralblood	blood
26	chr9:100403400-100434400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr9:100403400-100439600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr9:100403400-100444200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:100403600-100453800	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr9:100403800-100436200	Strong transcription	Adipose Nuclei	Adipose
31	chr9:100403800-100439000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
32	chr9:100404000-100435800	Strong transcription	A549	lung
33	chr9:100404000-100449200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr9:100404400-100422200	Strong transcription	Primary neutrophils fromperipheralblood	blood
35	chr9:100404800-100455400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr9:100405000-100437800	Strong transcription	GM12878-XiMat	blood
37	chr9:100405800-100438600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr9:100406200-100424400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr9:100409400-100439800	Strong transcription	HMEC	breast
40	chr9:100409600-100433200	Strong transcription	Fetal Intestine Large	intestine
41	chr9:100409600-100440000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr9:100409800-100427800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr9:100410200-100437800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr9:100410200-100454000	Strong transcription	Fetal Muscle Trunk	muscle
45	chr9:100410600-100421600	Weak transcription	Aorta	Aorta
46	chr9:100410600-100426200	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr9:100410600-100426400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr9:100411200-100423000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:100411200-100451000	Strong transcription	Liver	Liver
50	chr9:100411400-100426200	Weak transcription	Esophagus	oesophagus

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