Variant report

Variant	rs58570889
Chromosome Location	chr9:21848531-21848532
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs56166190	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs67134687	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7026112	0.84[ASN][1000 genomes]
rs7042302	0.84[ASN][1000 genomes]
rs72691580	0.87[AMR][1000 genomes]
rs7856455	0.86[AMR][1000 genomes]
rs7871127	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529609	chr9:21708371-22537069	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv8426	chr9:21763810-22176200	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21832200-21852400	Weak transcription	Stomach Mucosa	stomach
2	chr9:21837200-21850400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:21838400-21849000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:21839400-21854400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr9:21840600-21849000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr9:21840800-21848800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr9:21841400-21858800	Weak transcription	Colonic Mucosa	Colon
8	chr9:21841600-21854200	Weak transcription	Hela-S3	cervix
9	chr9:21841600-21854400	Weak transcription	NHLF	lung
10	chr9:21841600-21854600	Weak transcription	NHDF-Ad	bronchial
11	chr9:21841600-21858400	Weak transcription	Spleen	Spleen
12	chr9:21841800-21848600	Weak transcription	Fetal Brain Male	brain
13	chr9:21841800-21848600	Weak transcription	Thymus	Thymus
14	chr9:21841800-21849200	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr9:21841800-21852200	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr9:21841800-21852200	Weak transcription	Pancreas	Pancrea
17	chr9:21841800-21852200	Weak transcription	HepG2	liver
18	chr9:21841800-21852400	Weak transcription	Small Intestine	intestine
19	chr9:21841800-21854600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr9:21841800-21854800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr9:21841800-21854800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr9:21841800-21855400	Weak transcription	Gastric	stomach
23	chr9:21841800-21856200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr9:21841800-21856400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr9:21841800-21858600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr9:21841800-21864600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr9:21842000-21848800	Weak transcription	Left Ventricle	heart
28	chr9:21842000-21850200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr9:21842000-21852800	Weak transcription	HMEC	breast
30	chr9:21842000-21854600	Weak transcription	HSMMtube	muscle
31	chr9:21842000-21854600	Weak transcription	NHEK	skin
32	chr9:21842000-21854600	Weak transcription	Osteobl	bone
33	chr9:21842000-21855000	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr9:21842000-21857800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr9:21842000-21858400	Weak transcription	Right Ventricle	heart
36	chr9:21845200-21849000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
37	chr9:21845200-21849000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr9:21845600-21849200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr9:21845800-21849600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
40	chr9:21846000-21854800	Weak transcription	Fetal Kidney	kidney
41	chr9:21846600-21849000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:21846600-21849600	ZNF genes & repeats	Fetal Intestine Small	intestine
43	chr9:21846600-21869800	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr9:21846800-21853200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr9:21847000-21849000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
46	chr9:21847000-21849400	ZNF genes & repeats	Fetal Muscle Leg	muscle
47	chr9:21847400-21849000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
48	chr9:21847400-21849000	ZNF genes & repeats	Colon Smooth Muscle	Colon
49	chr9:21847400-21849000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
50	chr9:21847400-21849400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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