Variant report

Variant	rs7583544
Chromosome Location	chr2:74447782-74447783
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:74446879..74448831-chr2:74595217..74597589,2	K562	blood:
2	chr2:74424339..74426059-chr2:74445713..74448571,3	MCF-7	breast:
3	chr2:74434810..74438446-chr2:74445370..74448587,3	MCF-7	breast:
4	chr2:74403803..74406060-chr2:74446250..74448222,2	MCF-7	breast:
5	chr2:74447215..74450146-chr2:74463449..74466578,3	K562	blood:
6	chr2:74447215..74450146-chr2:74463449..74465120,2	K562	blood:
7	chr2:74446614..74449007-chr2:74477377..74479575,2	K562	blood:

Variant related genes	Relation type
ENSG00000188687	Chromatin interaction
ENSG00000114978	Chromatin interaction
ENSG00000204843	Chromatin interaction
ENSG00000065911	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs2001802	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2034454	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7571842	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs895988	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3427010	chr2:74351730-74813541	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
2	nsv834261	chr2:74391709-74613720	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
3	esv3401140	chr2:74439333-74533696	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	esv3380034	chr2:74439354-74533666	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:74427400-74448400	Weak transcription	Brain Anterior Caudate	brain
2	chr2:74427400-74453000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr2:74427400-74453200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr2:74427400-74460200	Weak transcription	Brain Substantia Nigra	brain
5	chr2:74427400-74462000	Weak transcription	Brain Angular Gyrus	brain
6	chr2:74427400-74484400	Weak transcription	Fetal Lung	lung
7	chr2:74427800-74494200	Weak transcription	Brain Germinal Matrix	brain
8	chr2:74428000-74448600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr2:74428600-74449600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:74429000-74450600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr2:74429000-74453200	Weak transcription	Ovary	ovary
12	chr2:74429200-74452800	Weak transcription	Fetal Heart	heart
13	chr2:74433600-74448400	Weak transcription	Brain Hippocampus Middle	brain
14	chr2:74433800-74448400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:74433800-74449200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:74433800-74449200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:74433800-74449400	Strong transcription	NHEK	skin
18	chr2:74433800-74449600	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr2:74433800-74449800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr2:74433800-74461800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr2:74434000-74453000	Weak transcription	Psoas Muscle	Psoas
22	chr2:74434200-74449400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:74434200-74449800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr2:74434600-74448800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr2:74434800-74449000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr2:74434800-74449400	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr2:74434800-74449600	Strong transcription	A549	lung
28	chr2:74435200-74449000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr2:74435400-74449400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr2:74435600-74450000	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr2:74435800-74454000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr2:74436000-74450400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:74436000-74453000	Weak transcription	Stomach Mucosa	stomach
34	chr2:74437000-74449000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr2:74437600-74453000	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr2:74439000-74449400	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr2:74439200-74453800	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr2:74439800-74525200	Weak transcription	Fetal Brain Male	brain
39	chr2:74441000-74458600	Weak transcription	Fetal Intestine Small	intestine
40	chr2:74441800-74448400	Weak transcription	Spleen	Spleen
41	chr2:74441800-74453000	Weak transcription	Gastric	stomach
42	chr2:74441800-74453000	Weak transcription	Pancreas	Pancrea
43	chr2:74441800-74453800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr2:74441800-74453800	Weak transcription	Esophagus	oesophagus
45	chr2:74441800-74458200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr2:74441800-74466000	Weak transcription	Adipose Nuclei	Adipose
47	chr2:74441800-74490400	Weak transcription	Fetal Brain Female	brain
48	chr2:74442000-74448600	Weak transcription	Primary B cells from cord blood	blood
49	chr2:74442200-74450400	Weak transcription	NHDF-Ad	bronchial
50	chr2:74442200-74453200	Weak transcription	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links