Variant report

Variant	rs1168024
Chromosome Location	chr1:62949651-62949652
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	chr1:62945259..62948292-chr1:62948478..62951331,3	K562	blood:
2	chr1:62941072..62943901-chr1:62947529..62950113,2	K562	blood:

Variant related genes	Relation type
ENSG00000116641	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1168006	0.82[AFR][1000 genomes]
rs1168007	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1168012	0.83[YRI][hapmap]
rs1168084	0.83[YRI][hapmap]
rs1168101	0.83[YRI][hapmap]
rs1185619	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1748191	0.83[YRI][hapmap]
rs1781200	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs610119	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs614636	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs614665	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs626209	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs628385	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs631982	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6587977	0.82[AFR][1000 genomes]
rs7522249	0.83[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1817371	chr1:62901935-63129697	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv1829390	chr1:62931632-62997573	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62909800-62977000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:62915400-62966600	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr1:62916000-62977200	Weak transcription	Right Ventricle	heart
4	chr1:62916200-62960000	Weak transcription	Spleen	Spleen
5	chr1:62916200-62963200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr1:62916600-62976600	Weak transcription	Psoas Muscle	Psoas
7	chr1:62918800-62950000	Weak transcription	GM12878-XiMat	blood
8	chr1:62918800-62950800	Weak transcription	K562	blood
9	chr1:62919000-62959200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr1:62920000-62971000	Weak transcription	Thymus	Thymus
11	chr1:62920000-62980200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr1:62922600-62982000	Weak transcription	A549	lung
13	chr1:62923200-62979200	Weak transcription	Fetal Thymus	thymus
14	chr1:62934400-62981200	Weak transcription	Stomach Mucosa	stomach
15	chr1:62937400-62957200	Weak transcription	Colonic Mucosa	Colon
16	chr1:62937400-62960000	Weak transcription	Pancreas	Pancrea
17	chr1:62937600-62957000	Weak transcription	Lung	lung
18	chr1:62938000-62960000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:62938000-62966600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:62938800-62956600	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr1:62938800-62973800	Weak transcription	Esophagus	oesophagus
22	chr1:62939000-62957000	Weak transcription	HSMMtube	muscle
23	chr1:62939200-62978200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:62939600-62954800	Weak transcription	Fetal Stomach	stomach
25	chr1:62939600-62956600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr1:62939600-62999800	Weak transcription	Gastric	stomach
27	chr1:62939600-63040600	Weak transcription	Aorta	Aorta
28	chr1:62939800-62956800	Weak transcription	Left Ventricle	heart
29	chr1:62939800-62961600	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr1:62939800-63044400	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr1:62939800-63060200	Weak transcription	Small Intestine	intestine
32	chr1:62941000-62959200	Weak transcription	Colon Smooth Muscle	Colon
33	chr1:62941000-63001000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr1:62941200-62955800	Weak transcription	Fetal Muscle Trunk	muscle
35	chr1:62941200-62955800	Weak transcription	Fetal Muscle Leg	muscle
36	chr1:62941200-62956800	Weak transcription	Primary T cells from cord blood	blood
37	chr1:62941400-62953200	Weak transcription	Fetal Brain Male	brain
38	chr1:62941600-62950000	Weak transcription	Primary B cells from cord blood	blood
39	chr1:62941600-62950600	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr1:62941600-62956400	Weak transcription	HMEC	breast
41	chr1:62941600-62956800	Weak transcription	Brain Substantia Nigra	brain
42	chr1:62941600-62957000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:62941600-62959200	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr1:62941600-62959800	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr1:62941600-62975400	Weak transcription	NHLF	lung
46	chr1:62941600-62978600	Weak transcription	Rectal Smooth Muscle	rectum
47	chr1:62941600-62981400	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr1:62941600-62998200	Weak transcription	Fetal Heart	heart
49	chr1:62941600-63011800	Weak transcription	Brain Hippocampus Middle	brain
50	chr1:62941800-62950400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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