Variant report

Variant	rs2615023
Chromosome Location	chr11:15917004-15917005
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:15906179..15908578-chr11:15915178..15917306,2	K562	blood:
2	chr11:15914710..15917174-chr11:15920611..15923591,2	K562	blood:
3	chr11:15910536..15912312-chr11:15915422..15917800,2	MCF-7	breast:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10766290	0.83[AMR][1000 genomes]
rs10832528	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11023753	0.83[AMR][1000 genomes]
rs11023754	0.81[EUR][1000 genomes]
rs11023756	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11023757	0.81[AMR][1000 genomes]
rs11023763	0.83[AMR][1000 genomes]
rs11023766	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12270494	0.83[AMR][1000 genomes]
rs12270765	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12287547	0.92[AMR][1000 genomes]
rs12289250	0.83[AMR][1000 genomes]
rs12290232	0.81[AMR][1000 genomes]
rs12364139	0.83[AMR][1000 genomes]
rs1440702	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1440705	0.82[AMR][1000 genomes]
rs1440707	0.87[AMR][1000 genomes]
rs1866819	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1866820	0.84[AMR][1000 genomes]
rs2008923	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2119376	0.83[AMR][1000 genomes]
rs2196961	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2218204	0.84[AMR][1000 genomes]
rs2582309	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2615024	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756835	0.83[AMR][1000 genomes]
rs4756837	0.97[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4756839	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4757371	0.83[AMR][1000 genomes]
rs4757373	0.83[AMR][1000 genomes]
rs4757374	0.88[AMR][1000 genomes]
rs4757375	0.83[AMR][1000 genomes]
rs4757377	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7106197	0.92[AMR][1000 genomes]
rs7122245	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs732908	0.87[EUR][1000 genomes]
rs7481566	0.84[AMR][1000 genomes]
rs965476	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs982988	0.84[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832073	chr11:15822409-15984078	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15908200-15917800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr11:15910400-15922800	Weak transcription	Fetal Intestine Small	intestine
3	chr11:15914800-15917600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:15914800-15922200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:15915000-15923200	Weak transcription	Pancreas	Pancrea
6	chr11:15915000-15929200	Weak transcription	Esophagus	oesophagus
7	chr11:15915200-15917800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr11:15915200-15918800	Weak transcription	NH-A	brain
9	chr11:15915200-15919000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr11:15915200-15919000	Weak transcription	HMEC	breast
11	chr11:15915200-15922800	Weak transcription	Left Ventricle	heart
12	chr11:15915200-15923000	Weak transcription	Gastric	stomach
13	chr11:15915200-15923000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr11:15915200-15924800	Weak transcription	NHEK	skin
15	chr11:15915400-15918200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr11:15915400-15923000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr11:15915400-15923600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr11:15915600-15918800	Weak transcription	Hela-S3	cervix
19	chr11:15915800-15917200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr11:15915800-15917600	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr11:15915800-15917600	Weak transcription	Psoas Muscle	Psoas
22	chr11:15915800-15918800	Weak transcription	Osteobl	bone
23	chr11:15915800-15919200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr11:15915800-15928400	Weak transcription	Fetal Kidney	kidney
25	chr11:15916000-15917200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr11:15916000-15919000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:15916000-15919000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:15916000-15919000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:15916000-15919400	Weak transcription	HSMMtube	muscle
30	chr11:15916000-15922400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr11:15916000-15922600	Weak transcription	Fetal Heart	heart
32	chr11:15916000-15922600	Weak transcription	Ovary	ovary
33	chr11:15916200-15919400	Weak transcription	Spleen	Spleen
34	chr11:15916200-15922400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr11:15916600-15919200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:15916800-15917800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr11:15916800-15921200	Enhancers	Fetal Muscle Leg	muscle
38	chr11:15917000-15917200	Enhancers	K562	blood

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