Variant report

Variant	rs13214196
Chromosome Location	chr6:144017105-144017106
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:144015602..144018341-chr6:144021601..144023244,2	K562	blood:
2	chr6:144004544..144009046-chr6:144017005..144020189,4	K562	blood:
3	chr6:144011351..144015622-chr6:144016784..144019989,3	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11155311	0.89[JPT][hapmap]
rs11755709	0.93[ASN][1000 genomes]
rs12192270	0.88[TSI][hapmap]
rs12199447	0.93[ASN][1000 genomes]
rs12200809	0.88[ASN][1000 genomes]
rs12524982	0.85[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12525281	0.90[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12525974	0.85[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12527275	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12530178	0.94[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13191026	0.88[JPT][hapmap]
rs13192672	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13193972	0.93[ASN][1000 genomes]
rs13194278	0.90[CHB][hapmap];0.86[CHD][hapmap]
rs13199178	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13213692	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13219740	0.88[ASN][1000 genomes]
rs1338535	0.89[JPT][hapmap]
rs17291151	0.85[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1884172	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2051009	0.90[CEU][hapmap];0.89[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2328507	0.80[CHB][hapmap]
rs34775537	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62427376	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62427377	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6932482	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7744358	0.90[CHB][hapmap]
rs7760627	0.90[CHB][hapmap]
rs9484792	0.90[CHB][hapmap];0.86[CHD][hapmap]
rs9484795	0.90[CEU][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.84[EUR][1000 genomes]
rs9496738	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9496740	0.90[CEU][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758084	chr6:143916621-144079976	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759476	chr6:143916621-144079976	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv886737	chr6:144010570-144033992	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13214196	AIG1	cis	parietal	SCAN

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144005000-144020400	Weak transcription	Fetal Muscle Trunk	muscle
2	chr6:144006000-144017800	Weak transcription	Fetal Heart	heart
3	chr6:144010200-144019600	Weak transcription	Spleen	Spleen
4	chr6:144010400-144017800	Weak transcription	Ovary	ovary
5	chr6:144010400-144020000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:144011600-144053200	Weak transcription	Hela-S3	cervix
7	chr6:144011800-144017600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr6:144011800-144019600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:144011800-144019800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:144012200-144018600	Enhancers	Stomach Mucosa	stomach
11	chr6:144012200-144026800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr6:144012400-144018000	Enhancers	Fetal Stomach	stomach
13	chr6:144013200-144017600	Weak transcription	Osteobl	bone
14	chr6:144013400-144017800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:144013400-144017800	Weak transcription	NHDF-Ad	bronchial
16	chr6:144013800-144019200	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr6:144014000-144017200	Weak transcription	Aorta	Aorta
18	chr6:144014000-144017800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:144014000-144019600	Weak transcription	Placenta	Placenta
20	chr6:144014200-144018200	Enhancers	Stomach Smooth Muscle	stomach
21	chr6:144014200-144019800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr6:144014200-144019800	Weak transcription	Right Atrium	heart
23	chr6:144014200-144027800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr6:144014200-144039800	Weak transcription	Pancreas	Pancrea
25	chr6:144014400-144019000	Enhancers	HepG2	liver
26	chr6:144014400-144022600	Weak transcription	Fetal Intestine Large	intestine
27	chr6:144014600-144020200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr6:144014800-144017400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr6:144014800-144017400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr6:144014800-144017400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr6:144014800-144017800	Enhancers	HUVEC	blood vessel
32	chr6:144014800-144018000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:144014800-144018200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr6:144014800-144019000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr6:144014800-144020800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr6:144015000-144018200	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr6:144015000-144018200	Enhancers	Fetal Muscle Leg	muscle
38	chr6:144015000-144018400	Enhancers	Fetal Lung	lung
39	chr6:144015000-144019800	Enhancers	Colon Smooth Muscle	Colon
40	chr6:144015200-144018800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr6:144015400-144017800	Enhancers	K562	blood
42	chr6:144015400-144019800	Enhancers	Muscle Satellite Cultured Cells	--
43	chr6:144015400-144019800	Weak transcription	Gastric	stomach
44	chr6:144015400-144020000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:144015400-144020800	Weak transcription	Lung	lung
46	chr6:144015400-144034600	Weak transcription	Esophagus	oesophagus
47	chr6:144015600-144018200	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr6:144015600-144018200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr6:144015600-144018200	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr6:144015800-144017200	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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