Variant report

Variant	rs9461151
Chromosome Location	chr6:25387486-25387487
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	chr6:25367288..25370021-chr6:25385958..25387793,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10456322	1.00[JPT][hapmap]
rs10456323	1.00[JPT][hapmap]
rs11752017	0.89[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs11759560	1.00[JPT][hapmap]
rs11759648	0.89[CEU][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs12154021	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12192331	1.00[JPT][hapmap]
rs12192342	1.00[JPT][hapmap]
rs12203031	1.00[JPT][hapmap]
rs12203442	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes]
rs12207791	1.00[JPT][hapmap]
rs12211739	1.00[JPT][hapmap]
rs1410443	1.00[JPT][hapmap]
rs150533	1.00[JPT][hapmap]
rs184202	1.00[JPT][hapmap]
rs212927	1.00[JPT][hapmap]
rs212929	1.00[JPT][hapmap]
rs212931	1.00[JPT][hapmap]
rs212932	1.00[JPT][hapmap]
rs212935	1.00[JPT][hapmap]
rs212937	1.00[JPT][hapmap]
rs212939	1.00[JPT][hapmap]
rs212940	1.00[JPT][hapmap]
rs301377	1.00[JPT][hapmap]
rs441472	1.00[JPT][hapmap]
rs453181	1.00[JPT][hapmap]
rs485567	1.00[JPT][hapmap]
rs6902158	1.00[JPT][hapmap]
rs6927384	1.00[JPT][hapmap]
rs6931843	1.00[JPT][hapmap]
rs716796	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs716798	1.00[YRI][hapmap]
rs760865	1.00[JPT][hapmap]
rs7742338	1.00[JPT][hapmap]
rs7752524	1.00[JPT][hapmap]
rs7762537	1.00[JPT][hapmap]
rs7764258	1.00[JPT][hapmap]
rs9348685	1.00[JPT][hapmap]
rs9461159	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9467496	0.89[CEU][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883485	chr6:25259137-25437986	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv883486	chr6:25260434-25422369	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv883487	chr6:25280119-25508868	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv830612	chr6:25342408-25509758	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv601168	chr6:25346334-25393306	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9461151	LRRC16	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25370800-25388800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:25377400-25410600	Weak transcription	Gastric	stomach
3	chr6:25377800-25395600	Weak transcription	Pancreas	Pancrea
4	chr6:25378400-25389000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:25378800-25389000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr6:25378800-25389200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr6:25379800-25387800	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr6:25380200-25389000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:25382000-25389200	Weak transcription	Aorta	Aorta
10	chr6:25383000-25403600	Weak transcription	Right Atrium	heart
11	chr6:25383600-25405000	Weak transcription	Fetal Intestine Small	intestine
12	chr6:25384200-25391600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr6:25384600-25387600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:25384800-25390600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:25385600-25389200	Weak transcription	Left Ventricle	heart
16	chr6:25385600-25390400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr6:25386400-25390800	Enhancers	Fetal Thymus	thymus
18	chr6:25387000-25389400	Enhancers	Thymus	Thymus
19	chr6:25387000-25389800	Enhancers	Primary B cells from peripheral blood	blood
20	chr6:25387400-25388000	Enhancers	Primary B cells from cord blood	blood
21	chr6:25387400-25388000	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr6:25387400-25388000	Enhancers	GM12878-XiMat	blood
23	chr6:25387400-25388200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr6:25387400-25388200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:25387400-25388400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:25387400-25388400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr6:25387400-25388400	Enhancers	Primary T cells from cord blood	blood
28	chr6:25387400-25389200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:25387400-25389800	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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