Variant report

Variant	rs3960736
Chromosome Location	chr18:9628013-9628014
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:9627468..9629148-chr18:9631077..9633967,2	MCF-7	breast:
2	chr18:9627920..9630651-chr18:9632769..9635738,3	K562	blood:
3	chr18:9613984..9616177-chr18:9626000..9628106,2	K562	blood:
4	chr18:9616624..9619206-chr18:9627826..9630962,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000263627	Chromatin interaction
ENSG00000212572	Chromatin interaction
ENSG00000154845	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs17417941	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	esv3693417	chr18:9512985-9693638	Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv458024	chr18:9558240-9828448	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv576448	chr18:9558240-9828448	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv576449	chr18:9623052-9700382	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9617600-9630600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr18:9625200-9628200	Enhancers	NHEK	skin
3	chr18:9625600-9628200	Enhancers	Hela-S3	cervix
4	chr18:9626200-9628200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr18:9627000-9628200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr18:9627200-9628200	Enhancers	HMEC	breast
7	chr18:9627400-9628200	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr18:9627400-9628200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr18:9627400-9628200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr18:9627400-9628200	Enhancers	NHLF	lung
11	chr18:9627600-9628200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr18:9627600-9628200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr18:9627600-9628200	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr18:9627600-9628200	Enhancers	HSMMtube	muscle
15	chr18:9627800-9630600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr18:9627800-9630600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr18:9627800-9632200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr18:9628000-9629000	Enhancers	Placenta	Placenta
19	chr18:9628000-9630000	Weak transcription	NHDF-Ad	bronchial
20	chr18:9628000-9630400	Weak transcription	K562	blood
21	chr18:9628000-9630600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr18:9628000-9630600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr18:9628000-9630600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr18:9628000-9630600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr18:9628000-9631400	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr18:9628000-9631400	Weak transcription	Osteobl	bone
27	chr18:9628000-9631600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr18:9628000-9631600	Weak transcription	A549	lung
29	chr18:9628000-9631800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr18:9628000-9631800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr18:9628000-9631800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr18:9628000-9631800	Weak transcription	NH-A	brain
33	chr18:9628000-9632200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr18:9628000-9642800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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