Variant report

Variant	rs73074560
Chromosome Location	chr4:7648670-7648671
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:7647729..7649234-chr4:7649422..7652337,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs58116563	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916610	chr4:7238883-7731946	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	esv34156	chr4:7526515-7750588	Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv878570	chr4:7534603-7836835	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' 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	nsv491712	chr4:7582506-8155069	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv508272	chr4:7591967-7722112	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv878571	chr4:7637297-7743283	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7644600-7652600	Weak transcription	Brain Anterior Caudate	brain
2	chr4:7644800-7649600	Weak transcription	Ovary	ovary
3	chr4:7644800-7652600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr4:7644800-7652800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr4:7646000-7648800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr4:7646200-7648800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
7	chr4:7646600-7649400	Weak transcription	Duodenum Mucosa	Duodenum
8	chr4:7646600-7651200	Weak transcription	HSMMtube	muscle
9	chr4:7646600-7651400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:7646600-7652000	Weak transcription	Brain Substantia Nigra	brain
11	chr4:7646600-7656400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr4:7647000-7649600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr4:7647200-7649200	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr4:7647200-7651600	Enhancers	HepG2	liver
15	chr4:7647600-7649200	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr4:7647600-7650000	Bivalent Enhancer	Placenta	Placenta
17	chr4:7647800-7650000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr4:7648000-7649400	Weak transcription	Lung	lung
19	chr4:7648000-7649600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:7648000-7650000	Enhancers	Liver	Liver
21	chr4:7648200-7649200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr4:7648200-7654800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr4:7648200-7654800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:7648400-7648800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr4:7648400-7648800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:7648400-7649000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr4:7648400-7651200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr4:7648400-7652200	Weak transcription	Esophagus	oesophagus
29	chr4:7648400-7653600	Enhancers	HUVEC	blood vessel
30	chr4:7648400-7658000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr4:7648600-7648800	Enhancers	Colonic Mucosa	Colon
32	chr4:7648600-7649000	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr4:7648600-7649600	Weak transcription	Adipose Nuclei	Adipose
34	chr4:7648600-7652200	Enhancers	Spleen	Spleen
35	chr4:7648600-7653800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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