Variant report

Variant	rs73617472
Chromosome Location	chr13:110948683-110948684
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:110948351..110950288-chr13:110954842..110957509,2	K562	blood:

Extended variants
information (count: 7 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2029767	1.00[AMR][1000 genomes]
rs4771662	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs55997809	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58910650	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs903355	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	nsv1038914	chr13:110860219-111190104	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv1046423	chr13:110936104-111286607	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110920200-110951200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr13:110925400-110949000	Weak transcription	Fetal Kidney	kidney
3	chr13:110928600-110951000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr13:110936200-110951000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr13:110936200-110958800	Weak transcription	Gastric	stomach
6	chr13:110937000-110955400	Weak transcription	A549	lung
7	chr13:110937400-110951000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr13:110937400-110952000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr13:110937800-110950600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr13:110938000-110951200	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr13:110939200-110949400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr13:110939600-110951000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr13:110939600-110951400	Weak transcription	Fetal Intestine Large	intestine
14	chr13:110939800-110950800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr13:110940200-110949200	Weak transcription	Psoas Muscle	Psoas
16	chr13:110940400-110951200	Weak transcription	HSMMtube	muscle
17	chr13:110940400-110953600	Weak transcription	NHEK	skin
18	chr13:110941000-110951000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr13:110942200-110949000	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr13:110942200-110950000	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr13:110942400-110951200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr13:110942600-110949000	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr13:110943400-110951000	Weak transcription	Colonic Mucosa	Colon
24	chr13:110943600-110951000	Weak transcription	Esophagus	oesophagus
25	chr13:110943800-110951000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr13:110944400-110950000	Enhancers	Adipose Nuclei	Adipose
27	chr13:110945600-110949400	Enhancers	Colon Smooth Muscle	Colon
28	chr13:110945600-110955600	Weak transcription	Pancreas	Pancrea
29	chr13:110945800-110950000	Weak transcription	Fetal Intestine Small	intestine
30	chr13:110946600-110949200	Weak transcription	Right Ventricle	heart
31	chr13:110946600-110951000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr13:110946800-110949200	Weak transcription	Fetal Stomach	stomach
33	chr13:110946800-110949200	Weak transcription	Lung	lung
34	chr13:110946800-110950600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr13:110946800-110950800	Weak transcription	NHLF	lung
36	chr13:110946800-110951000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr13:110946800-110951000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:110946800-110951000	Weak transcription	Spleen	Spleen
39	chr13:110946800-110951200	Weak transcription	Aorta	Aorta
40	chr13:110947000-110949000	Weak transcription	HUVEC	blood vessel
41	chr13:110947000-110949000	Weak transcription	Osteobl	bone
42	chr13:110947000-110949400	Weak transcription	Fetal Heart	heart
43	chr13:110947400-110948800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr13:110947400-110952600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr13:110947600-110950600	Weak transcription	NHDF-Ad	bronchial
46	chr13:110947800-110948800	Enhancers	Fetal Muscle Leg	muscle
47	chr13:110947800-110949800	Enhancers	Ovary	ovary
48	chr13:110948000-110949800	Enhancers	Right Atrium	heart
49	chr13:110948200-110949000	Enhancers	Placenta	Placenta
50	chr13:110948200-110949200	Enhancers	Duodenum Smooth Muscle	Duodenum

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