Variant report

Variant	rs7809962
Chromosome Location	chr7:6446136-6446137
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:6445380..6448087-chr7:6488948..6490884,2	K562	blood:
2	chr7:6444358..6447267-chr7:6449792..6451395,2	K562	blood:
3	chr7:6433852..6441003-chr7:6442415..6446485,8	K562	blood:
4	chr7:6413599..6415567-chr7:6443758..6446728,2	K562	blood:
5	chr7:6442339..6447267-chr7:6447321..6451395,5	K562	blood:
6	chr7:6431775..6434050-chr7:6443689..6446584,2	K562	blood:

Variant related genes	Relation type
ENSG00000136238	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11975814	1.00[AMR][1000 genomes]
rs14627	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34832914	1.00[AMR][1000 genomes]
rs35258488	1.00[AMR][1000 genomes]
rs60055081	1.00[AMR][1000 genomes]
rs60151305	1.00[AMR][1000 genomes]
rs60209405	1.00[AMR][1000 genomes]
rs60487674	1.00[AMR][1000 genomes]
rs6947138	1.00[AMR][1000 genomes]
rs73674121	1.00[AMR][1000 genomes]
rs7781818	1.00[AMR][1000 genomes]
rs7805986	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948912	chr7:5803903-6623553	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv1034060	chr7:5814823-6745710	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription 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 miRNA target site	138 gene(s)	inside rSNPs	diseases
3	nsv538711	chr7:5814823-6745710	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
4	nsv1028242	chr7:5819084-6645024	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
5	nsv538712	chr7:5819084-6645024	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
6	nsv949531	chr7:5949371-6753694	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
7	nsv1020236	chr7:6248930-6690377	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv497874	chr7:6296768-6614902	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
9	nsv605999	chr7:6396719-6472881	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	esv1824738	chr7:6431933-6554222	Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
11	esv1825865	chr7:6431933-6554222	Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
12	nsv606000	chr7:6446027-6477002	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6426000-6456400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:6426000-6475600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:6426400-6457400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:6436200-6448200	Weak transcription	Small Intestine	intestine
5	chr7:6437200-6449000	Strong transcription	Fetal Stomach	stomach
6	chr7:6437400-6457400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:6437400-6457400	Strong transcription	Dnd41	blood
8	chr7:6437600-6470400	Strong transcription	Fetal Brain Female	brain
9	chr7:6437800-6450200	Strong transcription	Thymus	Thymus
10	chr7:6437800-6456400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
11	chr7:6437800-6457200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr7:6437800-6457400	Strong transcription	Primary B cells from peripheral blood	blood
13	chr7:6438000-6457400	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr7:6438000-6458000	Strong transcription	Osteobl	bone
15	chr7:6438000-6462400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr7:6438200-6450600	Strong transcription	Colonic Mucosa	Colon
17	chr7:6438600-6457200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr7:6438600-6457400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr7:6438600-6475600	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr7:6438800-6457400	Strong transcription	Primary T cells from cord blood	blood
21	chr7:6438800-6457600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr7:6438800-6462800	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr7:6439000-6456400	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr7:6439200-6456000	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr7:6439200-6456800	Strong transcription	NHDF-Ad	bronchial
26	chr7:6439200-6457200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
27	chr7:6439200-6457400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:6439400-6448800	Strong transcription	Fetal Intestine Large	intestine
29	chr7:6439400-6454200	Strong transcription	Spleen	Spleen
30	chr7:6439400-6457200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:6439400-6457400	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr7:6439400-6457400	Strong transcription	Fetal Muscle Trunk	muscle
33	chr7:6439400-6458000	Strong transcription	Fetal Muscle Leg	muscle
34	chr7:6439600-6447200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:6439600-6449400	Weak transcription	Psoas Muscle	Psoas
36	chr7:6439600-6456000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:6439600-6456600	Strong transcription	HUVEC	blood vessel
38	chr7:6439600-6456800	Strong transcription	Aorta	Aorta
39	chr7:6439600-6457000	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr7:6439600-6457000	Strong transcription	Sigmoid Colon	Sigmoid Colon
41	chr7:6439600-6457200	Strong transcription	Fetal Lung	lung
42	chr7:6439600-6457400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr7:6439600-6472400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr7:6439800-6454800	Strong transcription	Stomach Smooth Muscle	stomach
45	chr7:6439800-6457400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:6439800-6457400	Strong transcription	Liver	Liver
47	chr7:6439800-6457400	Strong transcription	Duodenum Mucosa	Duodenum
48	chr7:6439800-6474600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:6439800-6474600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:6439800-6477400	Strong transcription	Fetal Intestine Small	intestine

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