Variant report

Variant	rs1970401
Chromosome Location	chr1:180512815-180512816
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SPI1	chr1:180512557-180512866	HL-60	blood:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:180511395..180514188-chr1:180783985..180786756,2	K562	blood:
2	chr1:180512434..180513990-chr1:180599840..180601494,2	MCF-7	breast:
3	chr1:180511669..180514906-chr1:180530245..180533112,3	K562	blood:
4	chr1:180507839..180510458-chr1:180510629..180513153,2	K562	blood:
5	chr1:180511015..180513302-chr1:180517883..180519397,2	K562	blood:
6	chr1:180505841..180513650-chr1:180514886..180521271,14	K562	blood:
7	chr1:180505455..180510458-chr1:180510629..180513153,4	K562	blood:
8	chr1:180470537..180472654-chr1:180512131..180513964,2	MCF-7	breast:
9	chr1:180510781..180513155-chr1:180847874..180850004,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000266683	TF binding region
ENSG00000143324	Chromatin interaction
ENSG00000135847	Chromatin interaction
ENSG00000266683	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12565152	0.84[AMR][1000 genomes]
rs2153327	0.84[AMR][1000 genomes]
rs2331742	0.84[AMR][1000 genomes]
rs4652510	0.84[AMR][1000 genomes]
rs61811627	0.84[AMR][1000 genomes]
rs61811628	0.84[AMR][1000 genomes]
rs6425647	0.84[AMR][1000 genomes]
rs6665615	0.84[AMR][1000 genomes]
rs946634	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003359	chr1:180300936-180727561	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
2	nsv949311	chr1:180438895-180692815	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription 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	46 gene(s)	inside rSNPs	diseases
3	nsv872578	chr1:180510771-180842344	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180506200-180513200	Weak transcription	Pancreas	Pancrea
2	chr1:180507000-180514800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr1:180508000-180513200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:180508800-180513000	Enhancers	Fetal Heart	heart
5	chr1:180509400-180513400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:180510200-180516000	Weak transcription	Fetal Muscle Trunk	muscle
7	chr1:180510400-180513000	Enhancers	Fetal Brain Male	brain
8	chr1:180510400-180529400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:180511000-180513400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:180511200-180513400	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr1:180511200-180513400	Enhancers	Brain Anterior Caudate	brain
12	chr1:180511600-180513200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:180511600-180516200	Weak transcription	Psoas Muscle	Psoas
14	chr1:180511800-180521200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:180512000-180515800	Weak transcription	Left Ventricle	heart
16	chr1:180512200-180513200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr1:180512200-180513200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:180512200-180513200	Weak transcription	Ovary	ovary
19	chr1:180512200-180513200	Weak transcription	Right Ventricle	heart
20	chr1:180512200-180513400	Weak transcription	Aorta	Aorta
21	chr1:180512200-180516200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr1:180512200-180516600	Weak transcription	Fetal Brain Female	brain
23	chr1:180512200-180521200	Weak transcription	HSMMtube	muscle
24	chr1:180512400-180515800	Weak transcription	Right Atrium	heart
25	chr1:180512400-180517800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr1:180512600-180516200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:180512600-180516200	Weak transcription	Brain Germinal Matrix	brain
28	chr1:180512800-180513400	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr1:180512800-180517600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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