Variant report

Variant	rs4656881
Chromosome Location	chr1:160099377-160099378
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:160098805..160101465-chr1:160105602..160107369,2	K562	blood:

Variant related genes	Relation type
ENSG00000018625	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs4656249	1.00[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	esv3327316	chr1:159985477-160151281	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	esv1806746	chr1:160029416-160105927	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	29 gene(s)	inside rSNPs	diseases
3	esv1824420	chr1:160029416-160105927	Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	29 gene(s)	inside rSNPs	diseases
4	esv1843994	chr1:160029416-160105927	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv534066	chr1:160029416-160105986	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	29 gene(s)	inside rSNPs	diseases
6	esv1794281	chr1:160029416-160111565	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
7	esv1820784	chr1:160029416-160159395	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
8	nsv534165	chr1:160029416-160187302	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
9	nsv872490	chr1:160083012-160121488	Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
10	esv3453724	chr1:160098374-160136495	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
11	esv3453725	chr1:160098456-160136351	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160088000-160146200	Weak transcription	Spleen	Spleen
2	chr1:160088800-160107400	Weak transcription	Fetal Brain Female	brain
3	chr1:160090200-160104600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr1:160090600-160112600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:160092400-160112200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
6	chr1:160092800-160100800	Strong transcription	Fetal Stomach	stomach
7	chr1:160093600-160099800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:160093800-160101200	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr1:160093800-160101800	Weak transcription	Gastric	stomach
10	chr1:160093800-160106600	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr1:160094000-160112000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr1:160094600-160100800	Enhancers	HSMM	muscle
13	chr1:160094800-160110200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:160095000-160099400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:160095000-160103200	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr1:160095400-160108200	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr1:160097000-160100000	Genic enhancers	Brain Substantia Nigra	brain
18	chr1:160097000-160101400	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
19	chr1:160097000-160109800	Strong transcription	H1 Cell Line	embryonic stem cell
20	chr1:160097200-160099600	Enhancers	Brain Angular Gyrus	brain
21	chr1:160097200-160099800	Strong transcription	Aorta	Aorta
22	chr1:160097200-160100000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr1:160097200-160100200	Transcr. at gene 5' and 3'	Skeletal Muscle Female	skeletal muscle
24	chr1:160097200-160100800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
25	chr1:160097200-160100800	Genic enhancers	Left Ventricle	heart
26	chr1:160097200-160101400	Strong transcription	H9 Cell Line	embryonic stem cell
27	chr1:160097200-160103400	Enhancers	Psoas Muscle	Psoas
28	chr1:160097200-160103400	Enhancers	Right Atrium	heart
29	chr1:160097200-160112200	Weak transcription	Brain Germinal Matrix	brain
30	chr1:160097400-160099600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:160097400-160100600	Genic enhancers	Fetal Muscle Leg	muscle
32	chr1:160097400-160100600	Strong transcription	Ovary	ovary
33	chr1:160097400-160101400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
34	chr1:160097400-160101600	Weak transcription	Pancreas	Pancrea
35	chr1:160097400-160104800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:160097400-160107600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:160097600-160100800	Strong transcription	Brain Anterior Caudate	brain
38	chr1:160097800-160100400	Genic enhancers	HSMMtube	muscle
39	chr1:160098000-160099800	Strong transcription	Brain Cingulate Gyrus	brain
40	chr1:160098000-160102600	Strong transcription	Rectal Smooth Muscle	rectum
41	chr1:160098200-160099400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:160098200-160100200	Strong transcription	Stomach Smooth Muscle	stomach
43	chr1:160098200-160100400	Weak transcription	Esophagus	oesophagus
44	chr1:160098200-160100400	Weak transcription	Lung	lung
45	chr1:160098200-160102000	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr1:160098400-160099600	Weak transcription	HepG2	liver
47	chr1:160098400-160100200	Strong transcription	Brain Hippocampus Middle	brain
48	chr1:160098400-160103200	Strong transcription	Colon Smooth Muscle	Colon
49	chr1:160098600-160099400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:160098600-160099600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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