Variant report

Variant	rs373387367
Chromosome Location	chr3:67634638-67634639
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv470638	chr3:67367341-67814738	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv460700	chr3:67393629-67712970	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv590560	chr3:67393629-67712970	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Strong transcription Flanking Active TSS 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 miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv590561	chr3:67548852-67690626	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv3359258	chr3:67589615-67828274	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	esv275108	chr3:67633420-67640906	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67579400-67657600	Weak transcription	Pancreas	Pancrea
2	chr3:67582200-67637000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr3:67595000-67639400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr3:67598000-67644200	Weak transcription	NHLF	lung
5	chr3:67601800-67673000	Weak transcription	Fetal Heart	heart
6	chr3:67602200-67644200	Weak transcription	Gastric	stomach
7	chr3:67602200-67654800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr3:67602200-67655400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr3:67602200-67656000	Weak transcription	Fetal Muscle Trunk	muscle
10	chr3:67602400-67646200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr3:67602600-67635600	Weak transcription	Aorta	Aorta
12	chr3:67609200-67637000	Weak transcription	Ovary	ovary
13	chr3:67609400-67644000	Weak transcription	NHDF-Ad	bronchial
14	chr3:67612400-67697200	Weak transcription	Hela-S3	cervix
15	chr3:67614000-67658600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr3:67616600-67644200	Weak transcription	HSMM	muscle
17	chr3:67618600-67655600	Weak transcription	NH-A	brain
18	chr3:67620400-67639800	Weak transcription	Small Intestine	intestine
19	chr3:67621000-67637200	Weak transcription	HepG2	liver
20	chr3:67621200-67644200	Weak transcription	Esophagus	oesophagus
21	chr3:67621200-67657600	Weak transcription	Fetal Stomach	stomach
22	chr3:67621400-67640000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr3:67621400-67650400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr3:67621800-67639400	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr3:67621800-67640600	Weak transcription	Placenta	Placenta
26	chr3:67621800-67644000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr3:67621800-67658000	Weak transcription	Thymus	Thymus
28	chr3:67622000-67635600	Weak transcription	GM12878-XiMat	blood
29	chr3:67622000-67640800	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr3:67622000-67641400	Weak transcription	Duodenum Mucosa	Duodenum
31	chr3:67622000-67648800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr3:67622200-67657400	Weak transcription	Brain Substantia Nigra	brain
33	chr3:67622400-67635800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:67622400-67637000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr3:67622400-67647800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr3:67622600-67635400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr3:67622600-67644400	Weak transcription	HMEC	breast
38	chr3:67622800-67644000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr3:67623200-67636600	Weak transcription	A549	lung
40	chr3:67623400-67650000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr3:67624400-67643800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr3:67624400-67649200	Weak transcription	Fetal Intestine Large	intestine
43	chr3:67624800-67637200	Weak transcription	Liver	Liver
44	chr3:67624800-67643800	Weak transcription	Dnd41	blood
45	chr3:67624800-67649200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:67624800-67651000	Weak transcription	Adipose Nuclei	Adipose
47	chr3:67624800-67658200	Weak transcription	Fetal Intestine Small	intestine
48	chr3:67626000-67635600	Weak transcription	Psoas Muscle	Psoas
49	chr3:67627200-67655400	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr3:67627600-67649000	Weak transcription	NHEK	skin

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