Variant report

Variant	rs62578427
Chromosome Location	chr9:117835096-117835097
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1262054	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17241078	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17241442	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17241477	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17819299	0.85[EUR][1000 genomes]
rs17819466	0.82[EUR][1000 genomes]
rs2150101	0.85[EUR][1000 genomes]
rs4549855	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62578423	0.82[EUR][1000 genomes]
rs62578424	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62578425	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62578426	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62580463	1.00[ASN][1000 genomes]
rs62580479	1.00[ASN][1000 genomes]
rs62580481	1.00[ASN][1000 genomes]
rs62580505	1.00[ASN][1000 genomes]
rs7859964	1.00[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	nsv831696	chr9:117701582-117874150	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv615250	chr9:117768021-118012841	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916912	chr9:117770039-118014140	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117782400-117848200	Weak transcription	Brain Substantia Nigra	brain
2	chr9:117802200-117848200	Weak transcription	Spleen	Spleen
3	chr9:117815400-117859200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:117817800-117850600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr9:117819800-117848000	Weak transcription	Fetal Intestine Small	intestine
6	chr9:117821400-117840200	Weak transcription	Brain Cingulate Gyrus	brain
7	chr9:117822400-117854400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr9:117825400-117848000	Weak transcription	Lung	lung
9	chr9:117826400-117835800	Weak transcription	Aorta	Aorta
10	chr9:117826600-117835600	Weak transcription	HMEC	breast
11	chr9:117826800-117849400	Strong transcription	Osteobl	bone
12	chr9:117827000-117848600	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr9:117827000-117849200	Strong transcription	NHDF-Ad	bronchial
14	chr9:117827200-117835800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:117827200-117855200	Strong transcription	NH-A	brain
16	chr9:117827400-117849200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr9:117829400-117839200	Strong transcription	NHLF	lung
18	chr9:117829800-117838400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr9:117830400-117840800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr9:117830800-117838600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr9:117831800-117848000	Strong transcription	Stomach Smooth Muscle	stomach
22	chr9:117832400-117835600	Strong transcription	NHEK	skin
23	chr9:117832400-117838600	Strong transcription	Duodenum Smooth Muscle	Duodenum
24	chr9:117832400-117840600	Strong transcription	Fetal Stomach	stomach
25	chr9:117832400-117842400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:117832600-117839000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr9:117832800-117838600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr9:117833200-117835800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr9:117833400-117835200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr9:117833400-117835800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr9:117833800-117836200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr9:117833800-117840400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr9:117834000-117849400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr9:117834000-117849800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:117834200-117840400	Strong transcription	Fetal Muscle Trunk	muscle
36	chr9:117834200-117842000	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr9:117834400-117837000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
38	chr9:117834400-117837000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:117834400-117839000	Strong transcription	Fetal Muscle Leg	muscle
40	chr9:117834600-117838200	Weak transcription	Fetal Intestine Large	intestine
41	chr9:117834600-117838600	Weak transcription	Esophagus	oesophagus
42	chr9:117834600-117839000	Strong transcription	Colon Smooth Muscle	Colon
43	chr9:117834800-117836400	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr9:117834800-117840600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr9:117834800-117848600	Weak transcription	Duodenum Mucosa	Duodenum
46	chr9:117835000-117835800	Weak transcription	Fetal Lung	lung
47	chr9:117835000-117836400	Strong transcription	Rectal Smooth Muscle	rectum
48	chr9:117835000-117840200	Weak transcription	Fetal Kidney	kidney
49	chr9:117835000-117842400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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