Variant report

Variant	rs7677735
Chromosome Location	chr4:8353057-8353058
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:8347622..8350029-chr4:8351308..8354631,3	MCF-7	breast:
2	chr4:8346988..8348504-chr4:8352358..8355226,2	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs35021055	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35668769	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002794	chr4:8110083-8490934	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv878595	chr4:8154534-8390646	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv878601	chr4:8214767-8440951	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv878602	chr4:8214767-8448992	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv1009011	chr4:8225669-8424831	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv470013	chr4:8315938-8377058	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv878604	chr4:8315938-8618916	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv878605	chr4:8332057-8378959	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv878606	chr4:8349738-8377058	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv878607	chr4:8349738-8380857	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv878608	chr4:8349738-8386720	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8344600-8354000	Weak transcription	Left Ventricle	heart
2	chr4:8349000-8353400	Weak transcription	Brain Anterior Caudate	brain
3	chr4:8349000-8353600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr4:8349000-8353600	Weak transcription	Brain Substantia Nigra	brain
5	chr4:8349000-8357600	Weak transcription	Fetal Heart	heart
6	chr4:8349200-8353400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr4:8349400-8353800	Weak transcription	Brain Angular Gyrus	brain
8	chr4:8349600-8353800	Weak transcription	Right Ventricle	heart
9	chr4:8351400-8355400	Enhancers	Fetal Muscle Leg	muscle
10	chr4:8351400-8356400	Enhancers	Ovary	ovary
11	chr4:8351600-8354600	Enhancers	Spleen	Spleen
12	chr4:8351600-8355400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr4:8351600-8356000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr4:8351600-8362800	Enhancers	Placenta Amnion	Placenta Amnion
15	chr4:8351800-8354400	Enhancers	Adipose Nuclei	Adipose
16	chr4:8352000-8353400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr4:8352200-8355600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:8352400-8354400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:8352400-8355000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:8352400-8356200	Enhancers	Fetal Thymus	thymus
21	chr4:8352600-8353200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
22	chr4:8352600-8354800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr4:8352600-8355000	Enhancers	Fetal Stomach	stomach
24	chr4:8352800-8353800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr4:8352800-8353800	Enhancers	H1 Cell Line	embryonic stem cell
26	chr4:8352800-8354400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:8352800-8354400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr4:8352800-8354400	Enhancers	Brain Cingulate Gyrus	brain
29	chr4:8352800-8355000	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr4:8352800-8355200	Enhancers	Fetal Lung	lung
31	chr4:8352800-8355400	Enhancers	HSMMtube	muscle
32	chr4:8353000-8353200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:8353000-8353400	Enhancers	Aorta	Aorta
34	chr4:8353000-8353600	Enhancers	Brain Hippocampus Middle	brain
35	chr4:8353000-8353800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr4:8353000-8353800	Weak transcription	Gastric	stomach
37	chr4:8353000-8354000	Enhancers	Primary T cells from cord blood	blood
38	chr4:8353000-8354000	Enhancers	Fetal Kidney	kidney
39	chr4:8353000-8354200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:8353000-8354600	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr4:8353000-8354600	Enhancers	Right Atrium	heart
42	chr4:8353000-8354800	Bivalent Enhancer	HepG2	liver
43	chr4:8353000-8355200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
44	chr4:8353000-8356200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr4:8353000-8357400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links