Variant report

Variant	rs10840305
Chromosome Location	chr11:9821118-9821119
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	chr11:9814289..9816378-chr11:9820915..9822756,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1032550	0.95[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10770060	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10770064	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10770065	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840306	0.94[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11042493	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12788348	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1875029	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1983002	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1996794	0.90[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34328537	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs34690050	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35401279	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs360136	0.94[JPT][hapmap]
rs360137	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs360147	0.94[ASN][1000 genomes]
rs360157	0.95[CHB][hapmap];0.88[JPT][hapmap]
rs3751000	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs415895	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs429835	0.95[CEU][hapmap];0.84[CHB][hapmap];0.83[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs440377	0.84[ASN][1000 genomes]
rs4910063	0.90[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4910499	0.85[CHB][hapmap];0.95[JPT][hapmap]
rs7126913	0.92[CEU][hapmap];0.83[CHB][hapmap];0.92[JPT][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7934930	0.88[ASN][1000 genomes]
rs7935673	0.89[ASN][1000 genomes]
rs960909	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[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	nsv933855	chr11:9645441-10130519	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1053369	chr11:9647837-9876054	Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription 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	39 gene(s)	inside rSNPs	diseases
3	nsv553468	chr11:9667828-9827871	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking 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	35 gene(s)	inside rSNPs	diseases
4	nsv896987	chr11:9759918-9885849	Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	esv3384280	chr11:9766350-9911228	Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10840305	SWAP70	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9797400-9821800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr11:9799600-9823400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr11:9800200-9823800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:9801600-9823800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr11:9803000-9823400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:9803000-9823400	Weak transcription	Psoas Muscle	Psoas
7	chr11:9803200-9828600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:9803200-9828600	Weak transcription	Gastric	stomach
9	chr11:9803200-9828800	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr11:9806800-9821400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr11:9806800-9828600	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr11:9807200-9823200	Weak transcription	Fetal Heart	heart
13	chr11:9808400-9828800	Weak transcription	Fetal Kidney	kidney
14	chr11:9809600-9823000	Weak transcription	HMEC	breast
15	chr11:9809600-9828600	Weak transcription	Esophagus	oesophagus
16	chr11:9809600-9832600	Weak transcription	Colonic Mucosa	Colon
17	chr11:9809800-9823200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr11:9809800-9828000	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr11:9809800-9828600	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr11:9810000-9822400	Weak transcription	Rectal Smooth Muscle	rectum
21	chr11:9810000-9823200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr11:9810000-9823200	Weak transcription	NH-A	brain
23	chr11:9810000-9829200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr11:9810200-9822600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr11:9810200-9828400	Weak transcription	Primary T cells from cord blood	blood
26	chr11:9810200-9829200	Weak transcription	Fetal Brain Male	brain
27	chr11:9810800-9823200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr11:9810800-9828600	Weak transcription	Duodenum Mucosa	Duodenum
29	chr11:9810800-9829000	Weak transcription	Right Ventricle	heart
30	chr11:9811000-9828600	Weak transcription	Brain Cingulate Gyrus	brain
31	chr11:9811200-9824000	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr11:9811600-9822800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:9811600-9823000	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr11:9811600-9823400	Weak transcription	Brain Hippocampus Middle	brain
35	chr11:9811600-9824000	Weak transcription	Brain Substantia Nigra	brain
36	chr11:9811600-9828000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr11:9811600-9828600	Weak transcription	Dnd41	blood
38	chr11:9811600-9828600	Weak transcription	HUVEC	blood vessel
39	chr11:9811600-9828800	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr11:9811600-9828800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr11:9811800-9821200	Weak transcription	NHLF	lung
42	chr11:9811800-9822600	Weak transcription	Colon Smooth Muscle	Colon
43	chr11:9811800-9823200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr11:9811800-9823200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:9811800-9823200	Weak transcription	Brain Anterior Caudate	brain
46	chr11:9811800-9823200	Weak transcription	Fetal Muscle Leg	muscle
47	chr11:9811800-9823200	Weak transcription	NHEK	skin
48	chr11:9811800-9823400	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr11:9811800-9823400	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr11:9811800-9827200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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