Variant report

Variant	rs57928672
Chromosome Location	chr1:70735628-70735629
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	chr1:70734545..70736304-chr1:70736804..70739106,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs56688715	1.00[AMR][1000 genomes]
rs57627286	1.00[AMR][1000 genomes]
rs59856193	1.00[AMR][1000 genomes]
rs61084750	1.00[AMR][1000 genomes]
rs61493071	1.00[AMR][1000 genomes]
rs72917819	1.00[AMR][1000 genomes]
rs72917823	1.00[AMR][1000 genomes]
rs72921081	1.00[AMR][1000 genomes]
rs72929203	1.00[AMR][1000 genomes]
rs72929206	1.00[AMR][1000 genomes]
rs72929207	1.00[AMR][1000 genomes]
rs72929211	1.00[AMR][1000 genomes]
rs72929214	1.00[AMR][1000 genomes]
rs72929215	1.00[AMR][1000 genomes]
rs72929225	1.00[AMR][1000 genomes]
rs72929226	1.00[AMR][1000 genomes]
rs72929228	1.00[AMR][1000 genomes]
rs72929237	1.00[AMR][1000 genomes]
rs72929241	1.00[AMR][1000 genomes]
rs72929267	1.00[AMR][1000 genomes]
rs72929272	1.00[AMR][1000 genomes]
rs72929277	1.00[AMR][1000 genomes]
rs72929286	1.00[AMR][1000 genomes]
rs72929299	1.00[AMR][1000 genomes]

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	nsv1014292	chr1:70689215-70799065	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv999219	chr1:70730556-71014911	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70688000-70819200	Weak transcription	Esophagus	oesophagus
2	chr1:70700600-70738800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:70710800-70756200	Weak transcription	Aorta	Aorta
4	chr1:70714000-70767000	Weak transcription	HSMMtube	muscle
5	chr1:70714200-70756000	Weak transcription	Colonic Mucosa	Colon
6	chr1:70715600-70767800	Weak transcription	Small Intestine	intestine
7	chr1:70715800-70747200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:70715800-70756200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:70715800-70771000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr1:70716000-70775600	Weak transcription	Spleen	Spleen
11	chr1:70716200-70775200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr1:70716600-70739000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr1:70716800-70737800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr1:70716800-70769000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:70716800-70769400	Weak transcription	Right Ventricle	heart
16	chr1:70716800-70815800	Weak transcription	Brain Angular Gyrus	brain
17	chr1:70717000-70736400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:70717000-70740200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr1:70717000-70746200	Weak transcription	Brain Hippocampus Middle	brain
20	chr1:70717000-70755600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:70717000-70759000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr1:70717200-70759000	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr1:70717600-70736000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr1:70717600-70746000	Weak transcription	Fetal Brain Male	brain
25	chr1:70717600-70752200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr1:70717600-70755000	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr1:70717600-70765000	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr1:70717600-70780400	Weak transcription	Brain Substantia Nigra	brain
29	chr1:70717800-70758000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr1:70717800-70761200	Weak transcription	NHLF	lung
31	chr1:70717800-70765000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr1:70717800-70788200	Weak transcription	Brain Cingulate Gyrus	brain
33	chr1:70718000-70740400	Weak transcription	Hela-S3	cervix
34	chr1:70718000-70742000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:70718000-70746000	Weak transcription	Colon Smooth Muscle	Colon
36	chr1:70718200-70755800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr1:70719000-70758800	Weak transcription	HMEC	breast
38	chr1:70719200-70783800	Weak transcription	A549	lung
39	chr1:70719600-70735800	Weak transcription	HSMM	muscle
40	chr1:70722800-70745800	Weak transcription	Fetal Heart	heart
41	chr1:70723600-70756800	Weak transcription	Lung	lung
42	chr1:70728200-70736000	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr1:70728200-70739000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr1:70728600-70736200	Weak transcription	Duodenum Mucosa	Duodenum
45	chr1:70728600-70742000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr1:70728600-70747200	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr1:70728600-70756200	Weak transcription	NH-A	brain
48	chr1:70728600-70761400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr1:70728800-70737000	Weak transcription	HepG2	liver
50	chr1:70728800-70749600	Weak transcription	NHEK	skin

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