Variant report

Variant	rs74044449
Chromosome Location	chr14:37116840-37116841
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr14:37111085..37113026-chr14:37114318..37117125,2	MCF-7	breast:
2	chr14:37116820..37118183-chr14:37618958..37620155,6	MCF-7	breast:
3	chr14:37115106..37119062-chr14:37125097..37130192,4	K562	blood:
4	chr14:37107177..37110095-chr14:37113473..37116981,4	MCF-7	breast:
5	chr14:37115811..37118059-chr14:37119729..37122052,2	K562	blood:
6	chr14:37115310..37117842-chr14:37618181..37620146,4	MCF-7	breast:
7	chr14:37116649..37118063-chr14:37216346..37217730,4	MCF-7	breast:
8	chr14:37113050..37116916-chr14:37130582..37134618,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC25A21-1	chr14:37116288-37118642	ENSG00000258661.1

No data

Variant related genes	Relation type
ENSG00000198807	Chromatin interaction
ENSG00000258661	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11848520	1.00[AMR][1000 genomes]
rs56743797	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60475307	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74044447	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74044448	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74044456	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74044457	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040256	chr14:36501452-37172046	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv542040	chr14:36501452-37172046	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv1047290	chr14:36564568-37445157	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
4	nsv1037952	chr14:36670484-37294692	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
5	nsv542042	chr14:36670484-37294692	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
6	nsv1053685	chr14:36915643-37245920	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv917279	chr14:36953511-37146655	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv949612	chr14:36996206-37121633	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	esv3523585	chr14:37115226-37118074	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	esv3523596	chr14:37115226-37118074	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37114800-37118200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr14:37115800-37117600	Active TSS	Esophagus	oesophagus
3	chr14:37116000-37117600	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:37116000-37117600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
5	chr14:37116000-37117600	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:37116000-37117600	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:37116000-37117800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
8	chr14:37116000-37117800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr14:37116000-37117800	Bivalent/Poised TSS	Fetal Thymus	thymus
10	chr14:37116000-37118000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
11	chr14:37116000-37118000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
12	chr14:37116000-37118000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
13	chr14:37116000-37118000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
14	chr14:37116000-37118000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
15	chr14:37116200-37117000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:37116200-37117000	Bivalent Enhancer	Liver	Liver
17	chr14:37116200-37117000	Bivalent Enhancer	Fetal Lung	lung
18	chr14:37116200-37117000	Bivalent Enhancer	Left Ventricle	heart
19	chr14:37116200-37117000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
20	chr14:37116200-37117200	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr14:37116200-37117200	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr14:37116200-37117200	Flanking Bivalent TSS/Enh	Placenta Amnion	Placenta Amnion
23	chr14:37116200-37117200	Bivalent/Poised TSS	HSMM	muscle
24	chr14:37116200-37117400	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr14:37116200-37117400	Bivalent Enhancer	Fetal Heart	heart
26	chr14:37116200-37117600	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:37116200-37117600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
28	chr14:37116200-37117600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
29	chr14:37116200-37117600	Bivalent/Poised TSS	Thymus	Thymus
30	chr14:37116200-37117600	Bivalent/Poised TSS	NHDF-Ad	bronchial
31	chr14:37116200-37117800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr14:37116200-37117800	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr14:37116200-37117800	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
34	chr14:37116200-37117800	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr14:37116200-37117800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr14:37116200-37117800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr14:37116200-37117800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr14:37116200-37117800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
39	chr14:37116200-37117800	Flanking Active TSS	Pancreas	Pancrea
40	chr14:37116200-37117800	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
41	chr14:37116200-37117800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
42	chr14:37116200-37117800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
43	chr14:37116200-37117800	ZNF genes & repeats	Spleen	Spleen
44	chr14:37116200-37117800	Flanking Bivalent TSS/Enh	HMEC	breast
45	chr14:37116200-37117800	Bivalent/Poised TSS	HSMMtube	muscle
46	chr14:37116200-37118000	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr14:37116200-37118000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:37116400-37117000	Bivalent Enhancer	NH-A	brain
49	chr14:37116400-37117400	Bivalent Enhancer	Fetal Brain Male	brain
50	chr14:37116400-37117400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links