Variant report

Variant	rs73654293
Chromosome Location	chr9:97579722-97579723
allele	A/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:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:97577390..97585730-chr9:97765650..97771704,20	MCF-7	breast:
2	chr9:97542228..97547641-chr9:97578377..97583453,10	MCF-7	breast:
3	chr9:97577751..97580681-chr9:97667871..97670064,2	MCF-7	breast:
4	chr9:97563933..97571351-chr9:97576672..97582632,18	MCF-7	breast:
5	chr9:97562492..97588737-chr9:97670126..97691056,102	MCF-7	breast:
6	chr9:97543312..97547479-chr9:97579071..97582826,7	MCF-7	breast:
7	chr9:97579441..97581622-chr9:97750768..97752612,2	MCF-7	breast:
8	chr9:97577481..97583901-chr9:97765035..97772381,17	MCF-7	breast:
9	chr9:97572097..97590438-chr9:97672990..97690806,63	MCF-7	breast:
10	chr9:97571425..97578055-chr9:97578265..97583690,17	MCF-7	breast:
11	chr9:97579092..97582374-chr9:97582651..97585462,4	MCF-7	breast:
12	chr9:97579045..97581444-chr9:97644293..97648187,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000148120	Chromatin interaction
ENSG00000252153	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs55737548	0.85[AFR][1000 genomes]
rs55770541	1.00[AFR][1000 genomes]
rs55791673	1.00[AFR][1000 genomes]
rs55803034	1.00[AFR][1000 genomes]
rs56278112	1.00[AFR][1000 genomes]
rs56278300	1.00[AFR][1000 genomes]
rs56339551	1.00[AFR][1000 genomes]
rs56401778	1.00[AFR][1000 genomes]
rs56737677	1.00[AFR][1000 genomes]
rs56944863	1.00[AFR][1000 genomes]
rs57057766	1.00[AFR][1000 genomes]
rs58215103	1.00[AFR][1000 genomes]
rs58243774	0.84[AFR][1000 genomes]
rs58447292	1.00[AFR][1000 genomes]
rs58496340	1.00[AFR][1000 genomes]
rs58960897	1.00[AFR][1000 genomes]
rs59594201	1.00[AFR][1000 genomes]
rs60009927	1.00[AFR][1000 genomes]
rs60240962	0.91[AFR][1000 genomes]
rs72746517	1.00[AFR][1000 genomes]
rs72746526	1.00[AFR][1000 genomes]
rs72746527	1.00[AFR][1000 genomes]
rs72746543	1.00[AFR][1000 genomes]
rs72747021	0.84[AFR][1000 genomes]
rs73654269	1.00[AFR][1000 genomes]
rs73654270	1.00[AFR][1000 genomes]
rs73654274	1.00[AFR][1000 genomes]
rs73654285	1.00[AFR][1000 genomes]
rs73654291	1.00[AFR][1000 genomes]
rs73654292	1.00[AFR][1000 genomes]
rs73654294	1.00[AFR][1000 genomes]
rs73654295	0.92[AFR][1000 genomes]
rs73654296	1.00[AFR][1000 genomes]
rs73654297	1.00[AFR][1000 genomes]
rs73654298	1.00[AFR][1000 genomes]
rs73654299	1.00[AFR][1000 genomes]
rs73654300	1.00[AFR][1000 genomes]
rs73654301	1.00[AFR][1000 genomes]
rs73654302	1.00[AFR][1000 genomes]
rs7465900	1.00[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	nsv893596	chr9:97321172-97598966	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97563400-97584200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr9:97563600-97594400	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr9:97563800-97584200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:97564000-97580000	Weak transcription	Primary B cells from peripheral blood	blood
5	chr9:97564000-97589200	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr9:97564200-97580400	Weak transcription	K562	blood
7	chr9:97565200-97587000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr9:97565400-97584200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:97567400-97593400	Weak transcription	Thymus	Thymus
10	chr9:97568600-97581400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr9:97568600-97589000	Weak transcription	Liver	Liver
12	chr9:97568800-97581400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr9:97568800-97581400	Weak transcription	Fetal Brain Male	brain
14	chr9:97568800-97586800	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr9:97569000-97580200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:97569000-97583800	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr9:97569000-97584200	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr9:97569000-97584200	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr9:97569200-97581200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr9:97569200-97586400	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr9:97569200-97589000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr9:97569400-97581200	Weak transcription	Stomach Mucosa	stomach
23	chr9:97569400-97581400	Weak transcription	Small Intestine	intestine
24	chr9:97569400-97587600	Weak transcription	Brain Germinal Matrix	brain
25	chr9:97569400-97589600	Weak transcription	Fetal Thymus	thymus
26	chr9:97569600-97581200	Weak transcription	Brain Anterior Caudate	brain
27	chr9:97569600-97581400	Weak transcription	Brain Cingulate Gyrus	brain
28	chr9:97569600-97586200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr9:97569800-97581400	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr9:97570000-97594400	Weak transcription	Dnd41	blood
31	chr9:97570000-97601400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr9:97570400-97590400	Weak transcription	Duodenum Mucosa	Duodenum
33	chr9:97571200-97579800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr9:97571400-97580000	Weak transcription	Fetal Lung	lung
35	chr9:97571400-97584000	Weak transcription	Fetal Kidney	kidney
36	chr9:97571600-97581400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr9:97571800-97622600	Weak transcription	Primary B cells from cord blood	blood
38	chr9:97572000-97601600	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr9:97572400-97582000	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr9:97572400-97583600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:97572400-97588600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr9:97572600-97593600	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr9:97574000-97581200	Weak transcription	HepG2	liver
44	chr9:97574200-97590000	Weak transcription	Fetal Intestine Large	intestine
45	chr9:97574400-97588600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:97575200-97579800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr9:97575200-97579800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr9:97575200-97580000	Weak transcription	NH-A	brain
49	chr9:97575200-97587600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr9:97575400-97580000	Weak transcription	Hela-S3	cervix

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