Variant report

Variant	rs61521906
Chromosome Location	chr4:124341699-124341700
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:124340163..124342380-chr4:124343948..124346028,2	K562	blood:
2	chr4:124338250..124340040-chr4:124341621..124343166,2	K562	blood:
3	chr4:124340419..124342149-chr4:124342290..124345121,2	MCF-7	breast:

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17006914	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56887963	0.92[AFR][1000 genomes]
rs58406081	0.92[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs6534397	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs66917631	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72684649	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[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	nsv1006945	chr4:124206328-124503863	Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv537240	chr4:124206328-124503863	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	esv34581	chr4:124271321-125247395	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv595379	chr4:124337522-124395024	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124327000-124342800	Weak transcription	Right Atrium	heart
2	chr4:124332800-124343200	Enhancers	Primary hematopoietic stem cells	blood
3	chr4:124333800-124342600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr4:124337600-124342400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr4:124337800-124343000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr4:124339000-124343800	Enhancers	Fetal Intestine Large	intestine
7	chr4:124339200-124343800	Enhancers	Fetal Intestine Small	intestine
8	chr4:124339200-124349200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:124339400-124341800	Enhancers	Primary B cells from peripheral blood	blood
10	chr4:124339600-124342000	Enhancers	Thymus	Thymus
11	chr4:124340000-124342400	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr4:124340000-124344800	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr4:124340200-124342200	Weak transcription	K562	blood
14	chr4:124340200-124342400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr4:124340200-124342400	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr4:124340200-124342400	Weak transcription	Fetal Lung	lung
17	chr4:124340200-124342600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr4:124340200-124342600	Weak transcription	NHLF	lung
19	chr4:124340200-124342800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr4:124340200-124342800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr4:124340200-124342800	Weak transcription	Stomach Mucosa	stomach
22	chr4:124340400-124342000	Enhancers	HepG2	liver
23	chr4:124340400-124342400	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr4:124340400-124342400	Weak transcription	HSMM	muscle
25	chr4:124340400-124342600	Weak transcription	HUVEC	blood vessel
26	chr4:124340400-124343200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr4:124340400-124343600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr4:124340600-124342400	Weak transcription	Osteobl	bone
29	chr4:124340600-124342600	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr4:124340600-124342800	Weak transcription	Primary B cells from cord blood	blood
31	chr4:124340600-124343000	Weak transcription	GM12878-XiMat	blood
32	chr4:124340600-124343600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr4:124340600-124348200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:124340800-124341800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr4:124340800-124342600	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr4:124340800-124343000	Enhancers	Fetal Thymus	thymus
37	chr4:124340800-124343400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr4:124341000-124342400	Weak transcription	Hela-S3	cervix
39	chr4:124341600-124341800	Enhancers	Primary T cells from cord blood	blood
40	chr4:124341600-124341800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr4:124341600-124341800	Enhancers	Small Intestine	intestine
42	chr4:124341600-124342600	Enhancers	Duodenum Mucosa	Duodenum
43	chr4:124341600-124344400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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