Variant report

Variant	rs6730521
Chromosome Location	chr2:112783957-112783958
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	chr2:112782602..112784298-chr2:112789398..112791163,2	K562	blood:
2	chr2:112783217..112785127-chr2:113032960..113034634,2	K562	blood:

Variant related genes	Relation type
ENSG00000188177	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10199083	0.81[JPT][hapmap]
rs10207726	0.89[CHB][hapmap];0.83[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap]
rs1113419	1.00[CEU][hapmap];0.95[GIH][hapmap];0.90[TSI][hapmap];0.89[EUR][1000 genomes]
rs11884641	1.00[CEU][hapmap];0.89[CHB][hapmap];0.89[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11884693	0.95[CEU][hapmap];0.89[CHB][hapmap];0.89[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11887652	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11893308	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11902247	0.86[EUR][1000 genomes]
rs12469210	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12470338	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12474039	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12477716	0.95[CEU][hapmap];0.83[CHD][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes]
rs1400321	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs1400324	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs1400325	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs1516629	0.95[CEU][hapmap];0.83[CHD][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap]
rs17174870	0.95[CEU][hapmap];0.83[CHD][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap]
rs17175275	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17175331	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17835605	0.95[CEU][hapmap]
rs28377357	0.81[ASN][1000 genomes]
rs3811632	0.89[CHB][hapmap];0.83[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap]
rs3811640	0.81[CEU][hapmap];0.88[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4278932	1.00[CEU][hapmap];0.89[CHB][hapmap];0.89[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4349353	0.89[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4434006	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4491736	0.80[AMR][1000 genomes]
rs4521048	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4528767	1.00[CEU][hapmap];0.89[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4567941	0.86[GIH][hapmap];0.85[MEX][hapmap]
rs4848918	0.81[JPT][hapmap]
rs4848978	0.81[CEU][hapmap];0.86[GIH][hapmap]
rs55766181	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55792453	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55799805	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55812028	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55972521	0.81[EUR][1000 genomes]
rs56272510	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs57116599	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs57732600	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58065683	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58641606	0.80[EUR][1000 genomes]
rs59650987	0.81[EUR][1000 genomes]
rs61583444	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6710733	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6712080	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6713344	0.90[CEU][hapmap];0.86[GIH][hapmap];0.81[MEX][hapmap]
rs6725192	0.81[JPT][hapmap]
rs6737989	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6738237	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7563113	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7568632	0.95[CEU][hapmap];0.81[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes]
rs7575552	0.81[EUR][1000 genomes]
rs7578057	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs867311	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874863	chr2:112591224-113157344	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv874864	chr2:112617280-113104142	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv874865	chr2:112623098-113049274	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
4	nsv1013218	chr2:112645633-112908416	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	esv3333591	chr2:112669320-112892618	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	nsv1002027	chr2:112679182-112861534	Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv1014787	chr2:112679182-112908416	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS 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	nsv535893	chr2:112679182-112908416	Strong transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	nsv999746	chr2:112691270-112796083	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv1003129	chr2:112691270-112816694	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	esv2760607	chr2:112691282-112803423	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	nsv431491	chr2:112699350-112793981	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv515698	chr2:112699350-112795908	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
14	nsv933392	chr2:112747230-112792349	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6730521	IL1RN	cis	parietal	SCAN

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112713200-112790600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr2:112723400-112789200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr2:112733200-112789200	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr2:112753000-112784000	Weak transcription	Fetal Lung	lung
5	chr2:112755400-112789200	Weak transcription	Colon Smooth Muscle	Colon
6	chr2:112758200-112789600	Weak transcription	Fetal Kidney	kidney
7	chr2:112761800-112784000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr2:112765800-112789600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr2:112768000-112789200	Weak transcription	Brain Hippocampus Middle	brain
10	chr2:112768600-112789600	Weak transcription	Fetal Muscle Leg	muscle
11	chr2:112769000-112789000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:112769000-112789200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:112769200-112788400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr2:112769200-112789200	Weak transcription	Adipose Nuclei	Adipose
15	chr2:112769600-112791200	Weak transcription	Colonic Mucosa	Colon
16	chr2:112770200-112789400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr2:112770600-112787600	Weak transcription	Brain Angular Gyrus	brain
18	chr2:112771400-112786000	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr2:112771400-112789000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr2:112774400-112786400	Strong transcription	Liver	Liver
21	chr2:112774400-112790200	Weak transcription	Right Atrium	heart
22	chr2:112777200-112789200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr2:112777400-112786000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:112777400-112789400	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr2:112777600-112788800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr2:112777800-112784400	Strong transcription	HepG2	liver
27	chr2:112778800-112784400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr2:112778800-112784600	Strong transcription	Placenta Amnion	Placenta Amnion
29	chr2:112778800-112787200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:112779400-112787400	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr2:112780200-112786000	Weak transcription	Gastric	stomach
32	chr2:112780200-112789800	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr2:112780400-112784000	Weak transcription	K562	blood
34	chr2:112780400-112784200	Weak transcription	Primary hematopoietic stem cells	blood
35	chr2:112780400-112786000	Weak transcription	Left Ventricle	heart
36	chr2:112780400-112787600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr2:112780600-112789200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr2:112781400-112785800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr2:112781600-112784000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:112781600-112789000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr2:112781600-112789200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:112781600-112789200	Weak transcription	Brain Substantia Nigra	brain
43	chr2:112781600-112789200	Weak transcription	Placenta	Placenta
44	chr2:112781600-112790600	Weak transcription	Lung	lung
45	chr2:112782000-112789200	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr2:112782200-112789200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr2:112782800-112788200	Weak transcription	Fetal Muscle Trunk	muscle
48	chr2:112783000-112784800	Enhancers	HUVEC	blood vessel
49	chr2:112783000-112785800	Weak transcription	Stomach Smooth Muscle	stomach
50	chr2:112783000-112789200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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