Variant report

Variant	rs17241477
Chromosome Location	chr9:117827842-117827843
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	CEBPB	chr9:117827778-117827901	HepG2	liver:	n/a	chr9:117827826-117827843 chr9:117827829-117827840
2	CEBPB	chr9:117827739-117827938	A549	lung:	n/a	chr9:117827826-117827843 chr9:117827829-117827840
3	CEBPB	chr9:117827787-117827987	IMR90	lung:	n/a	chr9:117827826-117827843 chr9:117827829-117827840
4	CEBPB	chr9:117827819-117827861	K562	blood:	n/a	chr9:117827826-117827843 chr9:117827829-117827840

Variant related genes	Relation type
TNC	TF binding region

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10117421	1.00[CHB][hapmap]
rs1262054	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1330361	1.00[CHB][hapmap]
rs1537011	1.00[CHB][hapmap]
rs17241078	0.87[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes]
rs17241442	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes]
rs17819299	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes]
rs17819466	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2150101	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes]
rs4549855	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes]
rs62578423	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62578424	0.83[EUR][1000 genomes]
rs62578425	0.83[EUR][1000 genomes]
rs62578426	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62578427	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	chr9:117791600-117833200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr9:117802200-117848200	Weak transcription	Spleen	Spleen
4	chr9:117812800-117830600	Weak transcription	Fetal Lung	lung
5	chr9:117815400-117859200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:117817800-117850600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr9:117819800-117848000	Weak transcription	Fetal Intestine Small	intestine
8	chr9:117821400-117840200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr9:117822400-117854400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr9:117823200-117828000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:117824600-117828000	Strong transcription	Fetal Stomach	stomach
12	chr9:117825000-117828000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:117825200-117828000	Genic enhancers	Colon Smooth Muscle	Colon
14	chr9:117825400-117848000	Weak transcription	Lung	lung
15	chr9:117826000-117830600	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr9:117826000-117834200	Weak transcription	Fetal Kidney	kidney
17	chr9:117826400-117829800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr9:117826400-117833600	Weak transcription	HSMMtube	muscle
19	chr9:117826400-117834400	Weak transcription	Esophagus	oesophagus
20	chr9:117826400-117835800	Weak transcription	Aorta	Aorta
21	chr9:117826600-117828000	Strong transcription	NHLF	lung
22	chr9:117826600-117835600	Weak transcription	HMEC	breast
23	chr9:117826800-117828600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr9:117826800-117828800	Weak transcription	Fetal Intestine Large	intestine
25	chr9:117826800-117849400	Strong transcription	Osteobl	bone
26	chr9:117827000-117834800	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr9:117827000-117834800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr9:117827000-117848600	Strong transcription	Cortex derived primary cultured neurospheres	brain
29	chr9:117827000-117849200	Strong transcription	NHDF-Ad	bronchial
30	chr9:117827200-117828200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:117827200-117828200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:117827200-117829400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr9:117827200-117830400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr9:117827200-117832400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:117827200-117832400	Weak transcription	NHEK	skin
36	chr9:117827200-117832600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr9:117827200-117834200	Weak transcription	Fetal Muscle Trunk	muscle
38	chr9:117827200-117834400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr9:117827200-117835800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr9:117827200-117855200	Strong transcription	NH-A	brain
41	chr9:117827400-117828200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr9:117827400-117828400	Weak transcription	Fetal Muscle Leg	muscle
43	chr9:117827400-117828400	Weak transcription	Rectal Smooth Muscle	rectum
44	chr9:117827400-117829200	Weak transcription	Stomach Smooth Muscle	stomach
45	chr9:117827400-117832400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr9:117827400-117832600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr9:117827400-117832600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr9:117827400-117834400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr9:117827400-117849200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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