Variant report

Variant	rs67300176
Chromosome Location	chr7:97781243-97781244
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:97780327..97782025-chr7:97795539..97798023,2	K562	blood:
2	chr7:97781216..97783623-chr7:97806937..97808476,2	K562	blood:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10215815	0.85[AFR][1000 genomes]
rs10275267	0.81[AFR][1000 genomes]
rs72494441	0.85[AFR][1000 genomes]
rs754464	0.87[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031371	chr7:97312452-98070538	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv3500384	chr7:97527787-98015382	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
3	esv3500386	chr7:97527787-98015382	Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
4	nsv1017481	chr7:97597641-98041043	Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	nsv539031	chr7:97597641-98041043	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
6	nsv1019531	chr7:97653880-98034129	Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv539032	chr7:97653880-98034129	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	esv1816676	chr7:97676259-97868033	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv831066	chr7:97726879-97890550	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv1033029	chr7:97773232-98017992	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
11	nsv539033	chr7:97773232-98017992	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97745600-97781600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:97762600-97793000	Weak transcription	Fetal Heart	heart
3	chr7:97763200-97792600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:97763400-97801000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:97763400-97821000	Weak transcription	NHLF	lung
6	chr7:97763600-97788400	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr7:97763600-97793000	Weak transcription	NH-A	brain
8	chr7:97763600-97814200	Weak transcription	Osteobl	bone
9	chr7:97763600-97815800	Weak transcription	HSMM	muscle
10	chr7:97763800-97784000	Weak transcription	HUVEC	blood vessel
11	chr7:97764000-97806200	Weak transcription	Psoas Muscle	Psoas
12	chr7:97765800-97840800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr7:97766000-97795000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:97766200-97781600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:97766200-97790000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr7:97766400-97786000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:97766600-97798400	Weak transcription	HSMMtube	muscle
18	chr7:97767800-97781400	Weak transcription	GM12878-XiMat	blood
19	chr7:97767800-97781400	Weak transcription	HMEC	breast
20	chr7:97768200-97784200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr7:97768800-97807000	Weak transcription	Stomach Mucosa	stomach
22	chr7:97771800-97797800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr7:97772200-97781600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr7:97772400-97781600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr7:97772400-97784000	Weak transcription	NHDF-Ad	bronchial
26	chr7:97772400-97821600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr7:97772600-97781400	Weak transcription	Aorta	Aorta
28	chr7:97772600-97783400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:97772800-97784200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:97773000-97781400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:97773000-97781600	Weak transcription	Fetal Kidney	kidney
32	chr7:97773200-97781400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:97773200-97781600	Weak transcription	Brain Anterior Caudate	brain
34	chr7:97773200-97783800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:97773200-97784000	Weak transcription	Brain Substantia Nigra	brain
36	chr7:97773200-97784200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr7:97775600-97803600	Weak transcription	K562	blood
38	chr7:97777600-97789200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:97777800-97790600	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr7:97778000-97782000	Strong transcription	Hela-S3	cervix
41	chr7:97778000-97790000	Strong transcription	Primary T cells from cord blood	blood
42	chr7:97778600-97781400	Weak transcription	Gastric	stomach
43	chr7:97778600-97781400	Weak transcription	Rectal Smooth Muscle	rectum
44	chr7:97778600-97783400	Weak transcription	Primary hematopoietic stem cells	blood
45	chr7:97778800-97792800	Weak transcription	Small Intestine	intestine
46	chr7:97779000-97781400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr7:97779800-97789800	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr7:97780000-97789400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr7:97780200-97792000	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr7:97780400-97782400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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