Variant report

Variant	rs74090724
Chromosome Location	chr1:76198309-76198310
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NFYA	chr1:76198272-76198444	GM12878	blood:	n/a	n/a
2	POLR2A	chr1:76196918-76198892	K562	blood:	n/a	n/a
3	RFX5	chr1:76198124-76198537	K562	blood:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76197492..76199222-chr1:76216070..76218442,2	K562	blood:
2	chr1:76195849..76201919-chr1:76251987..76255873,8	K562	blood:
3	chr1:76196771..76198499-chr1:76258126..76260501,2	K562	blood:
4	chr1:76197028..76199654-chr1:76253368..76256114,2	K562	blood:
5	chr1:76188769..76191418-chr1:76197121..76200007,3	MCF-7	breast:
6	chr1:76196771..76202637-chr1:76258126..76262356,7	K562	blood:
7	chr1:76190052..76193339-chr1:76196508..76198872,3	K562	blood:
8	chr1:76197560..76200556-chr1:76208948..76211290,2	K562	blood:

No data

Variant related genes	Relation type
ACADM	TF binding region
ENSG00000181227	Chromatin interaction
ENSG00000201487	Chromatin interaction
ENSG00000178193	Chromatin interaction
ENSG00000206620	Chromatin interaction
ENSG00000117054	Chromatin interaction
ENSG00000207241	Chromatin interaction
ENSG00000137955	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10465725	1.00[EUR][1000 genomes]
rs11161872	0.82[EUR][1000 genomes]
rs1144329	0.92[EUR][1000 genomes]
rs1146603	0.92[EUR][1000 genomes]
rs1146605	0.92[EUR][1000 genomes]
rs1146606	0.92[EUR][1000 genomes]
rs1146608	0.92[EUR][1000 genomes]
rs1146611	0.92[EUR][1000 genomes]
rs1146612	0.92[EUR][1000 genomes]
rs1146614	0.92[EUR][1000 genomes]
rs1146615	0.92[EUR][1000 genomes]
rs1146618	0.92[EUR][1000 genomes]
rs1146619	0.92[EUR][1000 genomes]
rs1146620	0.92[EUR][1000 genomes]
rs1146622	0.92[EUR][1000 genomes]
rs1146624	0.92[EUR][1000 genomes]
rs1146628	0.92[EUR][1000 genomes]
rs1146629	0.92[EUR][1000 genomes]
rs1146641	0.92[EUR][1000 genomes]
rs12074938	1.00[EUR][1000 genomes]
rs12079065	1.00[EUR][1000 genomes]
rs12079211	1.00[EUR][1000 genomes]
rs12079950	0.82[EUR][1000 genomes]
rs12081631	1.00[EUR][1000 genomes]
rs12093817	0.92[EUR][1000 genomes]
rs12094698	0.92[EUR][1000 genomes]
rs13376397	1.00[EUR][1000 genomes]
rs17097567	1.00[EUR][1000 genomes]
rs17097707	0.82[EUR][1000 genomes]
rs17097710	1.00[EUR][1000 genomes]
rs55781251	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55977041	1.00[EUR][1000 genomes]
rs56036152	0.80[AMR][1000 genomes]
rs56069207	0.80[AMR][1000 genomes]
rs56322662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56364153	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs57443433	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs5745309	1.00[EUR][1000 genomes]
rs5745418	1.00[EUR][1000 genomes]
rs57798497	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58125729	1.00[EUR][1000 genomes]
rs59723961	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59932454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60219146	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs60630670	0.80[AMR][1000 genomes]
rs60871503	0.80[AMR][1000 genomes]
rs61124994	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61612438	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74088936	0.80[AMR][1000 genomes]
rs74088996	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs74088997	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs74088999	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs74090705	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs74090716	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74090717	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74090720	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74090726	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74090729	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74090734	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74090737	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74090744	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7512465	1.00[EUR][1000 genomes]
rs7544911	0.84[EUR][1000 genomes]
rs815310	0.82[EUR][1000 genomes]
rs815311	0.82[EUR][1000 genomes]
rs9970840	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519329	chr1:75830438-76358591	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv870520	chr1:76088392-76206490	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv830281	chr1:76095292-76251053	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv871572	chr1:76161889-76208488	Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76190800-76199400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:76190800-76207200	Weak transcription	Spleen	Spleen
3	chr1:76190800-76208000	Weak transcription	Gastric	stomach
4	chr1:76191000-76199000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:76191200-76219600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:76191400-76199200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr1:76191400-76199400	Weak transcription	Aorta	Aorta
8	chr1:76191800-76208000	Weak transcription	A549	lung
9	chr1:76191800-76208200	Weak transcription	Brain Substantia Nigra	brain
10	chr1:76191800-76209400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr1:76192000-76198600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr1:76192000-76198600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:76192000-76198600	Weak transcription	HSMMtube	muscle
14	chr1:76192000-76199400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr1:76192000-76199400	Weak transcription	Lung	lung
16	chr1:76192000-76208000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:76192000-76210200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:76192000-76220400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:76192000-76220600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr1:76192000-76227800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr1:76192200-76198400	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr1:76192200-76198800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:76192200-76199200	Weak transcription	Brain Hippocampus Middle	brain
24	chr1:76192200-76200000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr1:76192200-76200200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr1:76192200-76200400	Weak transcription	Placenta	Placenta
27	chr1:76192200-76204600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:76192200-76217800	Weak transcription	Fetal Brain Male	brain
29	chr1:76192200-76222000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr1:76192400-76198400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr1:76192400-76198400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr1:76192400-76198600	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr1:76192400-76198600	Weak transcription	Fetal Lung	lung
34	chr1:76192400-76198600	Weak transcription	HSMM	muscle
35	chr1:76192400-76198600	Weak transcription	NH-A	brain
36	chr1:76192400-76199200	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr1:76192400-76199400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr1:76192400-76199400	Weak transcription	Colon Smooth Muscle	Colon
39	chr1:76192400-76199400	Weak transcription	Thymus	Thymus
40	chr1:76192400-76199600	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr1:76192400-76200200	Weak transcription	HMEC	breast
42	chr1:76192400-76200200	Weak transcription	HUVEC	blood vessel
43	chr1:76192400-76200600	Weak transcription	Brain Angular Gyrus	brain
44	chr1:76192400-76200600	Weak transcription	Fetal Kidney	kidney
45	chr1:76192400-76200600	Weak transcription	Rectal Smooth Muscle	rectum
46	chr1:76192400-76201200	Weak transcription	Stomach Mucosa	stomach
47	chr1:76192400-76207600	Weak transcription	Colonic Mucosa	Colon
48	chr1:76192600-76199200	Weak transcription	NHEK	skin
49	chr1:76192600-76199400	Weak transcription	Stomach Smooth Muscle	stomach
50	chr1:76192800-76198600	Weak transcription	Fetal Muscle Leg	muscle

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