Variant report

Variant	rs182070891
Chromosome Location	chr13:80081384-80081385
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:80053689..80055771-chr13:80081076..80082958,2	K562	blood:

Variant related genes	Relation type
ENSG00000232132	Chromatin interaction
ENSG00000102471	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832657	chr13:79904978-80099108	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
2	nsv523979	chr13:79979679-80120263	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	nsv916983	chr13:80065879-80249702	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	esv3380861	chr13:80080701-80082699	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv8765	chr13:80081176-80081948	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv3405945	chr13:80081201-80082249	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv2229257	chr13:80081216-80081893	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv2651677	chr13:80081248-80082970	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv3513530	chr13:80081288-80081809	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv3488422	chr13:80081289-80081793	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	esv3488420	chr13:80081297-80081904	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	esv3488421	chr13:80081320-80081795	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
13	esv3513563	chr13:80081330-80081799	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	esv3513552	chr13:80081340-80081782	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	esv3488423	chr13:80081344-80081768	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
16	esv3513519	chr13:80081350-80081767	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
17	esv3018	chr13:80081378-80081980	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
18	esv3513541	chr13:80081379-80081713	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:80064800-80084800	Weak transcription	Fetal Intestine Small	intestine
2	chr13:80066800-80084000	Weak transcription	Pancreas	Pancrea
3	chr13:80066800-80122800	Weak transcription	Esophagus	oesophagus
4	chr13:80067200-80095000	Weak transcription	HSMM	muscle
5	chr13:80070600-80096600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr13:80076000-80099200	Weak transcription	Hela-S3	cervix
7	chr13:80076200-80082600	Weak transcription	Osteobl	bone
8	chr13:80076200-80093200	Weak transcription	HMEC	breast
9	chr13:80077600-80088800	Weak transcription	Brain Angular Gyrus	brain
10	chr13:80077600-80095600	Weak transcription	Fetal Intestine Large	intestine
11	chr13:80077800-80082600	Weak transcription	Small Intestine	intestine
12	chr13:80077800-80082800	Weak transcription	Right Atrium	heart
13	chr13:80077800-80089000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr13:80078000-80082400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr13:80078000-80097200	Weak transcription	Psoas Muscle	Psoas
16	chr13:80078000-80097800	Weak transcription	Ovary	ovary
17	chr13:80078200-80082400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr13:80078200-80082600	Weak transcription	Stomach Mucosa	stomach
19	chr13:80078200-80088600	Weak transcription	Fetal Heart	heart
20	chr13:80078200-80102000	Weak transcription	Right Ventricle	heart
21	chr13:80078800-80085800	Enhancers	Dnd41	blood
22	chr13:80079600-80086600	Weak transcription	Gastric	stomach
23	chr13:80079600-80098200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr13:80079800-80082600	Weak transcription	Left Ventricle	heart
25	chr13:80080000-80082200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr13:80080400-80082400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr13:80080600-80082400	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr13:80080800-80081400	Enhancers	NHEK	skin
29	chr13:80080800-80082200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr13:80081200-80082600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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