Variant report

Variant	rs9804328
Chromosome Location	chr10:50379825-50379826
allele	G/T
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	chr10:50379588-50379966	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:50378923..50381166-chr10:50424445..50426719,2	K562	blood:
2	chr10:50379304..50381161-chr10:50382104..50383879,2	MCF-7	breast:

Variant related genes	Relation type
C10orf128	TF binding region

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10219080	0.91[AMR][1000 genomes]
rs11100991	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12243870	1.00[AMR][1000 genomes]
rs12258104	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12258230	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12268209	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2246238	0.82[AMR][1000 genomes]
rs4442460	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4483511	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56737365	0.91[AMR][1000 genomes]
rs7067828	0.91[AMR][1000 genomes]
rs7067848	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7068517	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7068519	0.85[AFR][1000 genomes]
rs7077339	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7083685	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7095186	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73302715	0.91[AMR][1000 genomes]
rs73302716	0.91[AMR][1000 genomes]
rs73302759	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73304705	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73304711	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9804303	0.92[AFR][1000 genomes];1.00[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	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50359000-50382200	Weak transcription	Left Ventricle	heart
2	chr10:50362400-50380600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr10:50367600-50384600	Weak transcription	Dnd41	blood
4	chr10:50368200-50380800	Weak transcription	Esophagus	oesophagus
5	chr10:50369600-50380400	Weak transcription	Gastric	stomach
6	chr10:50372000-50384000	Weak transcription	Colonic Mucosa	Colon
7	chr10:50372800-50386200	Weak transcription	Pancreas	Pancrea
8	chr10:50373200-50385200	Weak transcription	Colon Smooth Muscle	Colon
9	chr10:50373600-50383000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr10:50375000-50384000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr10:50375400-50382600	Weak transcription	Lung	lung
12	chr10:50375800-50380600	Weak transcription	Brain Substantia Nigra	brain
13	chr10:50375800-50380600	Weak transcription	Right Atrium	heart
14	chr10:50376400-50381800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr10:50376800-50395200	Enhancers	Primary B cells from peripheral blood	blood
16	chr10:50377000-50380600	Weak transcription	Adipose Nuclei	Adipose
17	chr10:50377400-50381000	Enhancers	K562	blood
18	chr10:50377400-50382200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr10:50377600-50380600	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr10:50377800-50384000	Weak transcription	NHDF-Ad	bronchial
21	chr10:50378000-50381800	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr10:50378000-50386000	Enhancers	Fetal Muscle Leg	muscle
23	chr10:50378000-50388600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr10:50378200-50380600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr10:50378400-50380600	Weak transcription	Brain Hippocampus Middle	brain
26	chr10:50378600-50384800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr10:50378800-50380800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr10:50379200-50380000	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr10:50379200-50381000	Enhancers	Spleen	Spleen
30	chr10:50379200-50381600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr10:50379600-50380200	Enhancers	HSMMtube	muscle
32	chr10:50379600-50381000	Enhancers	Fetal Thymus	thymus
33	chr10:50379600-50382000	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr10:50379600-50383800	Enhancers	Primary B cells from cord blood	blood
35	chr10:50379800-50380000	Enhancers	Primary T cells fromperipheralblood	blood
36	chr10:50379800-50380000	Enhancers	Right Ventricle	heart
37	chr10:50379800-50380200	Enhancers	GM12878-XiMat	blood
38	chr10:50379800-50380400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr10:50379800-50380600	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr10:50379800-50382400	Enhancers	Skeletal Muscle Male	skeletal muscle

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