Variant report

Variant	rs10840307
Chromosome Location	chr11:9822250-9822251
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: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1045634	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10770061	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10840300	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10840301	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10840302	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10840304	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11042494	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11042495	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11042496	0.86[EUR][1000 genomes]
rs11042497	0.90[EUR][1000 genomes]
rs11042498	0.90[ASN][1000 genomes]
rs12786198	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16907071	0.96[ASN][1000 genomes]
rs360148	0.91[ASN][1000 genomes]
rs360149	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3751001	0.88[ASN][1000 genomes]
rs3763862	0.92[ASN][1000 genomes]
rs3829252	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4910500	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4910501	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4910502	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4910503	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4910505	0.87[EUR][1000 genomes]
rs55934784	0.91[ASN][1000 genomes]
rs7102804	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7105203	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7113459	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7120754	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7124706	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7925875	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7936721	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9795085	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9795121	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9795122	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9795123	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9799600-9823400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr11:9800200-9823800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:9801600-9823800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr11:9803000-9823400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr11:9803000-9823400	Weak transcription	Psoas Muscle	Psoas
6	chr11:9803200-9828600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:9803200-9828600	Weak transcription	Gastric	stomach
8	chr11:9803200-9828800	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr11:9806800-9828600	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr11:9807200-9823200	Weak transcription	Fetal Heart	heart
11	chr11:9808400-9828800	Weak transcription	Fetal Kidney	kidney
12	chr11:9809600-9823000	Weak transcription	HMEC	breast
13	chr11:9809600-9828600	Weak transcription	Esophagus	oesophagus
14	chr11:9809600-9832600	Weak transcription	Colonic Mucosa	Colon
15	chr11:9809800-9823200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr11:9809800-9828000	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr11:9809800-9828600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr11:9810000-9822400	Weak transcription	Rectal Smooth Muscle	rectum
19	chr11:9810000-9823200	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr11:9810000-9823200	Weak transcription	NH-A	brain
21	chr11:9810000-9829200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr11:9810200-9822600	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr11:9810200-9828400	Weak transcription	Primary T cells from cord blood	blood
24	chr11:9810200-9829200	Weak transcription	Fetal Brain Male	brain
25	chr11:9810800-9823200	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr11:9810800-9828600	Weak transcription	Duodenum Mucosa	Duodenum
27	chr11:9810800-9829000	Weak transcription	Right Ventricle	heart
28	chr11:9811000-9828600	Weak transcription	Brain Cingulate Gyrus	brain
29	chr11:9811200-9824000	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr11:9811600-9822800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:9811600-9823000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr11:9811600-9823400	Weak transcription	Brain Hippocampus Middle	brain
33	chr11:9811600-9824000	Weak transcription	Brain Substantia Nigra	brain
34	chr11:9811600-9828000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr11:9811600-9828600	Weak transcription	Dnd41	blood
36	chr11:9811600-9828600	Weak transcription	HUVEC	blood vessel
37	chr11:9811600-9828800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr11:9811600-9828800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr11:9811800-9822600	Weak transcription	Colon Smooth Muscle	Colon
40	chr11:9811800-9823200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr11:9811800-9823200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr11:9811800-9823200	Weak transcription	Brain Anterior Caudate	brain
43	chr11:9811800-9823200	Weak transcription	Fetal Muscle Leg	muscle
44	chr11:9811800-9823200	Weak transcription	NHEK	skin
45	chr11:9811800-9823400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr11:9811800-9823400	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr11:9811800-9827200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr11:9811800-9827800	Weak transcription	Fetal Thymus	thymus
49	chr11:9811800-9827800	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr11:9811800-9828400	Weak transcription	Rectal Mucosa Donor 29	rectum

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