Variant report

Variant	rs74042197
Chromosome Location	chr14:31733960-31733961
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:31732131..31735050-chr14:31739245..31741338,2	K562	blood:
2	chr14:31675532..31678117-chr14:31730710..31734144,6	MCF-7	breast:
3	chr14:31673985..31677853-chr14:31730006..31735257,8	MCF-7	breast:
4	chr14:31674477..31677310-chr14:31731984..31734716,2	K562	blood:

Variant related genes	Relation type
ENSG00000092148	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10141820	0.94[ASN][1000 genomes]
rs41436351	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs74042191	0.94[ASN][1000 genomes]
rs74042192	0.94[ASN][1000 genomes]
rs74042194	0.94[ASN][1000 genomes]
rs74042199	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][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	nsv901587	chr14:31501505-31752664	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2830427	chr14:31639110-32000034	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1050597	chr14:31711248-31904761	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31726400-31736000	Enhancers	Liver	Liver
2	chr14:31727200-31735000	Weak transcription	Gastric	stomach
3	chr14:31729400-31736200	Enhancers	Stomach Mucosa	stomach
4	chr14:31730400-31735800	Enhancers	NHLF	lung
5	chr14:31730600-31734000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:31730600-31734200	Enhancers	Hela-S3	cervix
7	chr14:31730800-31734000	Enhancers	Placenta Amnion	Placenta Amnion
8	chr14:31731000-31734000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr14:31731000-31734000	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr14:31731000-31734200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr14:31731000-31735400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr14:31731000-31735600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr14:31731000-31735800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr14:31731000-31735800	Enhancers	HMEC	breast
15	chr14:31731000-31736000	Enhancers	NHEK	skin
16	chr14:31731400-31735200	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr14:31731600-31734000	Enhancers	HUVEC	blood vessel
18	chr14:31731600-31735000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr14:31731600-31735000	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr14:31731800-31734000	Enhancers	Colon Smooth Muscle	Colon
21	chr14:31732200-31734800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr14:31732200-31735000	Weak transcription	Brain Anterior Caudate	brain
23	chr14:31732200-31735000	Weak transcription	Brain Hippocampus Middle	brain
24	chr14:31732200-31735200	Weak transcription	Fetal Kidney	kidney
25	chr14:31732200-31736000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr14:31732600-31736000	Enhancers	Fetal Intestine Large	intestine
27	chr14:31732800-31734000	Enhancers	Ovary	ovary
28	chr14:31732800-31735600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr14:31732800-31736000	Enhancers	Fetal Intestine Small	intestine
30	chr14:31733000-31734000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr14:31733000-31734600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr14:31733200-31734000	Enhancers	Small Intestine	intestine
33	chr14:31733200-31735200	Weak transcription	Right Atrium	heart
34	chr14:31733200-31735400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr14:31733400-31734000	Enhancers	A549	lung
36	chr14:31733400-31734400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr14:31733400-31734800	Weak transcription	K562	blood
38	chr14:31733400-31735000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr14:31733400-31736200	Enhancers	NHDF-Ad	bronchial
40	chr14:31733400-31737000	Weak transcription	HSMMtube	muscle
41	chr14:31733400-31739400	Weak transcription	Esophagus	oesophagus
42	chr14:31733600-31734200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr14:31733600-31734200	Enhancers	NH-A	brain
44	chr14:31733600-31735000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr14:31733600-31735000	Weak transcription	GM12878-XiMat	blood
46	chr14:31733600-31735200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr14:31733600-31735600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr14:31733600-31736400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr14:31733800-31735000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr14:31733800-31735000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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