Variant report

Variant	rs531987721
Chromosome Location	chr7:40624198-40624199
allele	A/G
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	nsv1030648	chr7:40218618-41032599	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1030515	chr7:40501867-40634808	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv887987	chr7:40505382-40748650	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv830971	chr7:40523075-40700172	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1025605	chr7:40623026-40789063	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv538823	chr7:40623026-40789063	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40611800-40626000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:40612800-40624600	Weak transcription	NHLF	lung
3	chr7:40619400-40626000	Weak transcription	HSMM	muscle
4	chr7:40619600-40624200	Weak transcription	Osteobl	bone
5	chr7:40619600-40624400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:40619600-40624400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:40619600-40624400	Weak transcription	NH-A	brain
8	chr7:40619600-40624600	Weak transcription	Dnd41	blood
9	chr7:40619600-40630200	Weak transcription	Aorta	Aorta
10	chr7:40620400-40624400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:40621000-40626000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:40622200-40625800	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr7:40622400-40624200	Weak transcription	HUVEC	blood vessel
14	chr7:40622600-40625600	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr7:40622600-40625800	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr7:40623200-40624800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr7:40623200-40624800	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr7:40623200-40625000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr7:40623200-40625000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:40623200-40626400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr7:40623200-40626400	Enhancers	HMEC	breast
22	chr7:40623200-40626400	Enhancers	NHDF-Ad	bronchial
23	chr7:40623400-40624600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr7:40623400-40625000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr7:40623400-40625000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr7:40623400-40625000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr7:40623400-40625200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:40623400-40626800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:40623600-40624400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr7:40623800-40624200	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr7:40623800-40624800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr7:40624000-40625000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr7:40624000-40625000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr7:40624000-40625400	Enhancers	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links