Variant report

Variant	rs9621298
Chromosome Location	chr22:32019104-32019105
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	22:32012966-32043914..22:32347255-32351014	K562	blood:
2	22:31936958-31958600..22:32012966-32043914	GM12878	blood:
3	22:32012966-32043914..22:32513817-32522138	K562	blood:
4	chr22:32017352..32019493-chr22:32020509..32023823,4	MCF-7	breast:
5	22:31829733-31836635..22:32012966-32043914	GM12878	blood:
6	chr22:32014846..32016763-chr22:32018159..32020204,2	MCF-7	breast:
7	22:32012966-32043914..22:32665993-32670527	K562	blood:
8	22:31930706-31935473..22:32012966-32043914	GM12878	blood:
9	22:32012966-32043914..22:32529813-32538538	K562	blood:
10	chr22:32007884..32012411-chr22:32016194..32020167,5	MCF-7	breast:
11	22:32012966-32043914..22:32846948-32860159	K562	blood:
12	chr22:32010251..32014501-chr22:32014940..32019879,7	MCF-7	breast:
13	chr22:31982507..31985125-chr22:32018725..32020856,2	MCF-7	breast:
14	22:32012966-32043914..22:32360288-32405313	K562	blood:

No data

Variant related genes	Relation type
ENSG00000230866	Chromatin interaction
ENSG00000184708	Chromatin interaction
ENSG00000241878	Chromatin interaction
ENSG00000238910	Chromatin interaction
ENSG00000234479	Chromatin interaction
ENSG00000239674	Chromatin interaction
ENSG00000229169	Chromatin interaction
ENSG00000214093	Chromatin interaction
ENSG00000240647	Chromatin interaction
ENSG00000232707	Chromatin interaction
ENSG00000198089	Chromatin interaction
ENSG00000224050	Chromatin interaction
ENSG00000184459	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10154415	1.00[AMR][1000 genomes]
rs10222293	0.88[AFR][1000 genomes]
rs12165610	1.00[AMR][1000 genomes]
rs12166668	1.00[AMR][1000 genomes]
rs12166752	1.00[AMR][1000 genomes]
rs12167269	1.00[AMR][1000 genomes]
rs12167380	1.00[AMR][1000 genomes]
rs12167999	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12169596	1.00[AMR][1000 genomes]
rs12170049	1.00[AMR][1000 genomes]
rs13433570	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16989611	1.00[AMR][1000 genomes]
rs16989642	1.00[AMR][1000 genomes]
rs16989647	1.00[AMR][1000 genomes]
rs16989655	1.00[AMR][1000 genomes]
rs28374120	1.00[AMR][1000 genomes]
rs28760352	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56662300	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5749296	1.00[AMR][1000 genomes]
rs57955202	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60117275	1.00[AMR][1000 genomes]
rs60746452	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61049980	1.00[AMR][1000 genomes]
rs61323004	1.00[AMR][1000 genomes]
rs73396261	1.00[AMR][1000 genomes]
rs73396267	1.00[AMR][1000 genomes]
rs73396277	1.00[AMR][1000 genomes]
rs73396290	1.00[AMR][1000 genomes]
rs73396301	1.00[AMR][1000 genomes]
rs73398213	1.00[AMR][1000 genomes]
rs73398220	1.00[AMR][1000 genomes]
rs7364312	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73881392	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73881394	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73881395	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73881396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73881398	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9619201	1.00[AMR][1000 genomes]
rs9619202	1.00[AMR][1000 genomes]
rs9619209	1.00[AMR][1000 genomes]
rs9619213	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9619214	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9619216	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9619227	1.00[AMR][1000 genomes]
rs9619228	1.00[AMR][1000 genomes]
rs9619236	1.00[AMR][1000 genomes]
rs9621271	1.00[AMR][1000 genomes]
rs9621273	1.00[AMR][1000 genomes]
rs9621274	1.00[AMR][1000 genomes]
rs9621276	1.00[AMR][1000 genomes]
rs9621277	1.00[AMR][1000 genomes]
rs9621281	1.00[AMR][1000 genomes]
rs9621283	1.00[AMR][1000 genomes]
rs9621284	1.00[AMR][1000 genomes]
rs9621293	1.00[AMR][1000 genomes]
rs9621297	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9621302	0.84[AFR][1000 genomes]
rs9621306	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9621308	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9621310	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9621314	1.00[AMR][1000 genomes]
rs9621320	1.00[AMR][1000 genomes]
rs9621337	1.00[AMR][1000 genomes]
rs9621342	1.00[AMR][1000 genomes]
rs9621343	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv914980	chr22:31966274-32024980	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv517534	chr22:31977594-32024980	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv829176	chr22:31998223-32029556	Strong transcription Weak transcription Enhancers Active TSS Flanking 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	20 gene(s)	inside rSNPs	diseases
4	esv1845516	chr22:32010436-32024552	Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	esv2830290	chr22:32011225-32057964	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31976400-32019200	Weak transcription	Fetal Brain Male	brain
2	chr22:31996600-32020600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr22:31998600-32022000	Weak transcription	Fetal Kidney	kidney
4	chr22:32003600-32022000	Strong transcription	Dnd41	blood
5	chr22:32008000-32021200	Weak transcription	Fetal Heart	heart
6	chr22:32008000-32022600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr22:32009600-32021800	Strong transcription	Primary T cells from cord blood	blood
8	chr22:32010200-32025600	Genic enhancers	Placenta	Placenta
9	chr22:32011400-32020000	Strong transcription	Fetal Stomach	stomach
10	chr22:32012200-32019800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr22:32012200-32020600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr22:32012200-32022600	Strong transcription	Thymus	Thymus
13	chr22:32012400-32020200	Strong transcription	Fetal Thymus	thymus
14	chr22:32012600-32019800	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr22:32012600-32020000	Strong transcription	Right Ventricle	heart
16	chr22:32012600-32020400	Strong transcription	Liver	Liver
17	chr22:32012600-32020800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr22:32012600-32022000	Weak transcription	Psoas Muscle	Psoas
19	chr22:32012600-32024400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr22:32012800-32019600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr22:32012800-32019800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr22:32012800-32020800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr22:32012800-32020800	Strong transcription	Lung	lung
24	chr22:32012800-32021400	Weak transcription	Right Atrium	heart
25	chr22:32012800-32021400	Strong transcription	NHLF	lung
26	chr22:32013000-32019200	Strong transcription	Osteobl	bone
27	chr22:32013000-32019400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr22:32013000-32022200	Strong transcription	Muscle Satellite Cultured Cells	--
29	chr22:32013200-32019400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr22:32013200-32019600	Strong transcription	Esophagus	oesophagus
31	chr22:32013200-32019800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr22:32013200-32020000	Strong transcription	Primary B cells from peripheral blood	blood
33	chr22:32013200-32020600	Strong transcription	Gastric	stomach
34	chr22:32013200-32020800	Weak transcription	Stomach Mucosa	stomach
35	chr22:32013200-32022000	Strong transcription	Sigmoid Colon	Sigmoid Colon
36	chr22:32013200-32024000	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr22:32013400-32020000	Strong transcription	GM12878-XiMat	blood
38	chr22:32013600-32019200	Strong transcription	HepG2	liver
39	chr22:32013600-32025200	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr22:32014000-32025600	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr22:32014200-32019800	Strong transcription	Fetal Muscle Leg	muscle
42	chr22:32014400-32019200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr22:32015000-32019200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr22:32015000-32022000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr22:32015200-32019200	Strong transcription	Stomach Smooth Muscle	stomach
46	chr22:32015200-32021400	Strong transcription	NHEK	skin
47	chr22:32015200-32021800	Strong transcription	Duodenum Mucosa	Duodenum
48	chr22:32015200-32022000	Weak transcription	Fetal Lung	lung
49	chr22:32015400-32022400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr22:32015400-32025200	Weak transcription	Hela-S3	cervix

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