Variant report

Variant	rs1950836
Chromosome Location	chr14:42076745-42076746
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SIN3A	chr14:42073598-42077869	H1-hESC	embryonic stem cell:	n/a	chr14:42077621-42077630 chr14:42076170-42076179 chr14:42075971-42075982
2	CTBP2	chr14:42074050-42077848	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr14:42075624-42077921	H1-neurons	neurons:	n/a	n/a
4	REST	chr14:42074960-42077937	H1-neurons	neurons:	n/a	chr14:42077585-42077598 chr14:42076936-42076956 chr14:42076170-42076180 chr14:42077503-42077513 chr14:42076268-42076278 chr14:42075096-42075104 chr14:42077314-42077327 chr14:42076038-42076056
5	POLR2A	chr14:42075639-42077939	H1-neurons	neurons:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:42076710-42076760	HL-60	blood:	n/a
2	chr14:42076710-42076760	HIPEpiC	eye:	n/a
3	chr14:42076710-42076760	PrEC	prostate:	n/a
4	chr14:42076710-42076760	SKMC	muscle:	n/a
5	chr14:42076710-42076760	AG09319	gingival:	n/a
6	chr14:42076710-42076760	A549	lung:	n/a
7	chr14:42076710-42076760	AG04450	lung:	fetal
8	chr14:42076710-42076760	LNCaP	prostate:	n/a
9	chr14:42076710-42076760	AG09309	skin:	n/a
10	chr14:42076710-42076760	HepG2	liver:	n/a
11	chr14:42076710-42076760	MCF10A-Er-Src	breast:	n/a
12	chr14:42076710-42076760	AG10803	skin:	n/a
13	chr14:42076710-42076760	SK-N-MC	brain:	n/a
14	chr14:42076710-42076760	HEEpiC	esophagus:	n/a
15	chr14:42076710-42076760	Jurkat	blood:	n/a
16	chr14:42076710-42076760	NT2-D1	testis:	n/a
17	chr14:42076710-42076760	MCF-7	breast:	n/a
18	chr14:42076710-42076760	U87	brain:	n/a
19	chr14:42076710-42076760	SK-N-SH_RA	brain:	n/a
20	chr14:42076710-42076760	HRE	kidney:	n/a
21	chr14:42076710-42076760	SK-N-SH	brain:	n/a
22	chr14:42076710-42076760	K562	blood:	n/a
23	chr14:42076710-42076760	AG04449	skin:	fetal
24	chr14:42076710-42076760	ovcar-3	ovarian:	n/a
25	chr14:42076710-42076760	GM12891	blood:	n/a
26	chr14:42076710-42076760	AoSMC	blood vessel:	n/a
27	chr14:42076710-42076760	HRCEpiC	kidney:	n/a
28	chr14:42076710-42076760	ECC-1	luminal epithelium:	n/a
29	chr14:42076710-42076760	PANC-1	pancreas:	n/a
30	chr14:42076710-42076760	HCM	heart:	n/a
31	chr14:42076710-42076760	T-47D	breast:	n/a
32	chr14:42076710-42076760	BE2_C	brain:	n/a
33	chr14:42076710-42076760	GM12878	blood:	n/a
34	chr14:42076710-42076760	NHDF-neo	bronchial:	n/a
35	chr14:42076710-42076760	NB4	blood:	n/a
36	chr14:42076710-42076760	GM12892	blood:	n/a
37	chr14:42076710-42076760	H1-hESC	embryonic stem cell:	embryo
38	chr14:42076710-42076760	HCT-116	colon:	n/a
39	chr14:42076710-42076760	HCPEpiC	choroid plexus:	n/a
40	chr14:42076710-42076760	GM06990	blood:	n/a
41	chr14:42076710-42076760	HUVEC	blood vessel:	n/a
42	chr14:42076710-42076760	HAEpiC	amniotic membrane:	n/a
43	chr14:42076710-42076760	HNPCEpiC	eye:	n/a
44	chr14:42076710-42076760	HCF	heart:	n/a
45	chr14:42076710-42076760	HRPEpiC	eye:	n/a
46	chr14:42076710-42076760	CMK	blood:	n/a
47	chr14:42076710-42076760	Hepatocyte	liver:	n/a
48	chr14:42076710-42076760	PFSK-1	brain:	n/a
49	chr14:42076710-42076760	RPTEC	kidney:	n/a
50	chr14:42076710-42076760	NH-A	brain:	n/a

No data

Variant related genes	Relation type
LRFN5	TF binding region
ENSG00000258636	TF binding region
LRFN5	CpG island
ENSG00000258636	CpG island

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10483526	0.85[EUR][1000 genomes]
rs1111177	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1111179	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11157241	0.80[EUR][1000 genomes]
rs1137567	0.85[EUR][1000 genomes]
rs12431444	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12589043	0.85[ASN][1000 genomes]
rs12589112	0.81[ASN][1000 genomes]
rs1609735	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17112133	0.82[ASN][1000 genomes]
rs17112137	0.81[ASN][1000 genomes]
rs17781288	0.86[EUR][1000 genomes]
rs1950831	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1950834	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1950835	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1950838	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1956450	0.85[EUR][1000 genomes]
rs1998126	0.81[ASN][1000 genomes]
rs2899928	0.84[ASN][1000 genomes]
rs4356390	0.85[EUR][1000 genomes]
rs58845274	0.81[ASN][1000 genomes]
rs61990286	0.86[EUR][1000 genomes]
rs61990288	0.86[EUR][1000 genomes]
rs61990289	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6572099	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7148091	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72684563	0.83[EUR][1000 genomes]
rs8003822	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8007172	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8013655	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047300	chr14:41671653-42361098	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv1831164	chr14:41673017-42103168	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv533968	chr14:41882101-42327882	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1042078	chr14:41993985-42120143	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2758353	chr14:42045873-42259511	Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	esv2759983	chr14:42045873-42259511	ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42070200-42076800	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr14:42070800-42077000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr14:42071400-42079800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr14:42072000-42078000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
5	chr14:42072800-42077000	Active TSS	Fetal Kidney	kidney
6	chr14:42073000-42077200	Active TSS	Ovary	ovary
7	chr14:42073000-42079600	Active TSS	Right Atrium	heart
8	chr14:42073200-42076800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr14:42073400-42076800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
10	chr14:42073600-42078400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
11	chr14:42073600-42079800	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
12	chr14:42073800-42076800	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr14:42073800-42076800	Bivalent/Poised TSS	Osteobl	bone
14	chr14:42073800-42077600	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
15	chr14:42073800-42077800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
16	chr14:42073800-42077800	Bivalent/Poised TSS	Left Ventricle	heart
17	chr14:42074000-42077400	Bivalent/Poised TSS	Fetal Thymus	thymus
18	chr14:42074000-42077800	Bivalent/Poised TSS	Psoas Muscle	Psoas
19	chr14:42074000-42078200	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
20	chr14:42074200-42076800	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr14:42074200-42077600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr14:42074400-42077800	Bivalent/Poised TSS	NHLF	lung
23	chr14:42074800-42077800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
24	chr14:42074800-42079800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:42075000-42078200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
26	chr14:42075200-42076800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr14:42075200-42076800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr14:42075200-42076800	Bivalent/Poised TSS	Brain Anterior Caudate	brain
29	chr14:42075200-42077600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr14:42075200-42077800	Active TSS	Placenta Amnion	Placenta Amnion
31	chr14:42075200-42079200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
32	chr14:42075400-42077600	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr14:42075400-42077800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr14:42075600-42076800	Bivalent/Poised TSS	HUVEC	blood vessel
35	chr14:42075600-42077000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr14:42075600-42077000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
37	chr14:42075600-42077000	Active TSS	NHDF-Ad	bronchial
38	chr14:42075600-42077200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr14:42075600-42077400	Bivalent/Poised TSS	Primary B cells from cord blood	blood
40	chr14:42075600-42077600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
41	chr14:42075600-42077600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr14:42075600-42077800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
43	chr14:42075800-42076800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr14:42075800-42076800	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
45	chr14:42075800-42077000	Bivalent/Poised TSS	A549	lung
46	chr14:42075800-42077200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:42075800-42077200	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
48	chr14:42076000-42076800	Active TSS	Aorta	Aorta
49	chr14:42076000-42077000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr14:42076000-42077200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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