Variant report

Variant	rs551545286
Chromosome Location	chr10:93967512-93967513
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	chr10:93967417-93967644	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:93967344..93971211-chr10:94049163..94052466,3	MCF-7	breast:
2	chr10:93958713..93960977-chr10:93966306..93968107,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000221042	TF binding region
ENSG00000198060	Chromatin interaction
ENSG00000107864	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv975763	chr10:93822289-94105956	Enhancers Bivalent Enhancer Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1046258	chr10:93866969-94466106	Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	esv2761614	chr10:93960695-93981177	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv948139	chr10:93966694-93969883	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 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	chr10:93926400-93976000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr10:93926600-93976000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr10:93926800-93982400	Weak transcription	HSMMtube	muscle
4	chr10:93927000-93970800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr10:93927200-93967600	Weak transcription	Adipose Nuclei	Adipose
6	chr10:93927200-93980400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr10:93927400-93970800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr10:93927400-93997800	Weak transcription	Fetal Intestine Large	intestine
9	chr10:93929200-93984800	Weak transcription	Fetal Intestine Small	intestine
10	chr10:93929400-93967800	Weak transcription	Colon Smooth Muscle	Colon
11	chr10:93934200-93976200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr10:93940200-93971200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr10:93940600-93970800	Weak transcription	Fetal Stomach	stomach
14	chr10:93941800-93968000	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr10:93941800-93971200	Weak transcription	Primary B cells from peripheral blood	blood
16	chr10:93947800-93967800	Weak transcription	GM12878-XiMat	blood
17	chr10:93958200-93968400	Weak transcription	Right Atrium	heart
18	chr10:93958400-93967600	Weak transcription	Brain Anterior Caudate	brain
19	chr10:93958400-93981000	Weak transcription	Psoas Muscle	Psoas
20	chr10:93959000-93969800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr10:93959000-93985800	Weak transcription	Brain Substantia Nigra	brain
22	chr10:93960800-93970000	Weak transcription	Hela-S3	cervix
23	chr10:93960800-93970800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr10:93960800-93976000	Weak transcription	Gastric	stomach
25	chr10:93961000-93990800	Weak transcription	Spleen	Spleen
26	chr10:93961600-93972200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr10:93962000-93976400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr10:93963000-93976400	Weak transcription	Aorta	Aorta
29	chr10:93964200-93968400	Weak transcription	Esophagus	oesophagus
30	chr10:93964200-93968400	Weak transcription	Pancreas	Pancrea
31	chr10:93964200-93976200	Weak transcription	Right Ventricle	heart
32	chr10:93964200-93993000	Weak transcription	Fetal Brain Female	brain
33	chr10:93964200-93996000	Weak transcription	Brain Germinal Matrix	brain
34	chr10:93964200-93997600	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr10:93964400-93970000	Weak transcription	Brain Angular Gyrus	brain
36	chr10:93964400-93982400	Weak transcription	HSMM	muscle
37	chr10:93965000-93970000	Weak transcription	Rectal Smooth Muscle	rectum
38	chr10:93966400-93986200	Weak transcription	Ovary	ovary
39	chr10:93966800-93967600	Genic enhancers	Left Ventricle	heart
40	chr10:93967000-93967800	Strong transcription	Brain Cingulate Gyrus	brain
41	chr10:93967000-93968800	Enhancers	Brain Hippocampus Middle	brain
42	chr10:93967000-93968800	Enhancers	Stomach Mucosa	stomach
43	chr10:93967200-93968600	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr10:93967400-93967600	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr10:93967400-93967600	Enhancers	Lung	lung
46	chr10:93967400-93967600	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr10:93967400-93967600	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr10:93967400-93967800	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr10:93967400-93968800	Enhancers	Fetal Lung	lung
50	chr10:93967400-93986200	Weak transcription	Fetal Heart	heart

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