Variant report

Variant	rs9633705
Chromosome Location	chr10:98380545-98380546
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr10:98379904-98380950	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:98345353..98347090-chr10:98380383..98383295,2	K562	blood:

Variant related genes	Relation type
PIK3AP1	TF binding region
ENSG00000077147	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10882806	1.00[EUR][1000 genomes]
rs11188776	1.00[EUR][1000 genomes]
rs11188794	1.00[EUR][1000 genomes]
rs11188806	1.00[EUR][1000 genomes]
rs11188824	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3413353	chr10:98039370-98561524	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv895909	chr10:98354924-98382165	Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv532232	chr10:98360775-99141797	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98350800-98395600	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr10:98352400-98399400	Strong transcription	Primary B cells from peripheral blood	blood
3	chr10:98352600-98403000	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr10:98353000-98388400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr10:98353000-98403000	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr10:98354600-98388600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr10:98357800-98382000	Strong transcription	GM12878-XiMat	blood
8	chr10:98360400-98392800	Weak transcription	Thymus	Thymus
9	chr10:98362200-98389200	Strong transcription	Primary B cells from cord blood	blood
10	chr10:98363800-98392600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr10:98366000-98388400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr10:98366600-98392600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr10:98367400-98418600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr10:98371000-98382600	Strong transcription	Spleen	Spleen
15	chr10:98371000-98388600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr10:98371000-98389000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr10:98372200-98388600	Strong transcription	Primary hematopoietic stem cells	blood
18	chr10:98374400-98390200	Weak transcription	Small Intestine	intestine
19	chr10:98375600-98380800	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr10:98375800-98390200	Weak transcription	Adipose Nuclei	Adipose
21	chr10:98376400-98381200	Enhancers	Ovary	ovary
22	chr10:98376800-98381000	Enhancers	Right Atrium	heart
23	chr10:98377000-98380800	Enhancers	Fetal Lung	lung
24	chr10:98377200-98384400	Enhancers	Stomach Mucosa	stomach
25	chr10:98377400-98392600	Weak transcription	Esophagus	oesophagus
26	chr10:98378200-98392600	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr10:98378400-98381200	Enhancers	Right Ventricle	heart
28	chr10:98378600-98381000	Enhancers	Colonic Mucosa	Colon
29	chr10:98378600-98382000	Enhancers	Gastric	stomach
30	chr10:98378800-98381400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr10:98378800-98389400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr10:98378800-98392400	Weak transcription	Fetal Intestine Large	intestine
33	chr10:98378800-98392600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr10:98379000-98381800	Weak transcription	Brain Substantia Nigra	brain
35	chr10:98379000-98396200	Weak transcription	HepG2	liver
36	chr10:98379200-98387600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr10:98379400-98382000	Enhancers	K562	blood
38	chr10:98379600-98392600	Strong transcription	Liver	Liver
39	chr10:98379800-98380800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr10:98379800-98381000	Genic enhancers	Pancreas	Pancrea
41	chr10:98379800-98385400	Strong transcription	Placenta	Placenta
42	chr10:98379800-98392200	Weak transcription	Fetal Intestine Small	intestine
43	chr10:98380000-98381400	Weak transcription	Fetal Brain Male	brain
44	chr10:98380000-98381800	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr10:98380000-98381800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr10:98380000-98392600	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr10:98380200-98392400	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr10:98380400-98380800	Weak transcription	Lung	lung
49	chr10:98380400-98392600	Weak transcription	Duodenum Mucosa	Duodenum
50	chr10:98380400-98392600	Weak transcription	Rectal Mucosa Donor 31	rectum

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