Variant report

Variant	rs61469377
Chromosome Location	chr1:160920902-160920903
allele	C/T
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	CTCF	chr1:160920860-160921010	GM12865	blood:	n/a	n/a
2	CTCF	chr1:160920900-160921050	GM12867	blood:	n/a	n/a

Variant related genes	Relation type
ITLN2	TF binding region

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

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12058351	1.00[EUR][1000 genomes]
rs12059277	1.00[EUR][1000 genomes]
rs12082989	1.00[EUR][1000 genomes]
rs12087087	1.00[EUR][1000 genomes]
rs12087658	1.00[EUR][1000 genomes]
rs12090411	1.00[EUR][1000 genomes]
rs12094026	1.00[EUR][1000 genomes]
rs12094349	1.00[EUR][1000 genomes]
rs12095533	1.00[EUR][1000 genomes]
rs12095682	1.00[EUR][1000 genomes]
rs56187725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59397787	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6656542	1.00[EUR][1000 genomes]
rs6678883	1.00[EUR][1000 genomes]
rs6698072	1.00[EUR][1000 genomes]
rs74126638	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74126641	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74126650	1.00[AMR][1000 genomes]
rs7524859	1.00[EUR][1000 genomes]
rs7532566	1.00[EUR][1000 genomes]
rs790060	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs790061	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530077	chr1:160836448-161284904	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160916600-160921800	Enhancers	Fetal Intestine Large	intestine
2	chr1:160916800-160923800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr1:160917600-160921800	Enhancers	A549	lung
4	chr1:160918000-160921400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:160918000-160923800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr1:160918200-160921000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr1:160918200-160921200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:160918200-160923800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr1:160918400-160921600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr1:160918600-160921000	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr1:160918800-160921000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:160919000-160924000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr1:160919000-160924400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:160919400-160921800	Enhancers	Fetal Intestine Small	intestine
15	chr1:160919400-160923000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr1:160919600-160921600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr1:160919600-160921600	Enhancers	NHEK	skin
18	chr1:160919600-160924200	Enhancers	HMEC	breast
19	chr1:160919800-160921800	Enhancers	Ovary	ovary
20	chr1:160919800-160921800	Enhancers	Right Atrium	heart
21	chr1:160919800-160923200	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr1:160919800-160924000	Weak transcription	Fetal Heart	heart
23	chr1:160920000-160921000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr1:160920000-160921400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:160920000-160923600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:160920200-160924200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr1:160920400-160921200	Enhancers	Left Ventricle	heart
28	chr1:160920400-160921400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:160920400-160921400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr1:160920600-160921000	Weak transcription	HepG2	liver
31	chr1:160920600-160921400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:160920600-160922800	Weak transcription	Right Ventricle	heart
33	chr1:160920800-160921200	Enhancers	Fetal Muscle Leg	muscle
34	chr1:160920800-160921400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr1:160920800-160921800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:160920800-160921800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr1:160920800-160921800	Enhancers	Esophagus	oesophagus
38	chr1:160920800-160921800	Enhancers	Fetal Muscle Trunk	muscle

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