Variant report

Variant	rs9789634
Chromosome Location	chr2:38816074-38816075
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:38815771-38816134	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:38810772..38814090-chr2:38815738..38818660,3	MCF-7	breast:
2	chr2:38815999..38818648-chr2:38976723..38978521,3	K562	blood:
3	chr2:38814609..38816208-chr2:38972347..38974363,2	K562	blood:

Variant related genes	Relation type
HNRNPLL	TF binding region
ENSG00000115875	Chromatin interaction
ENSG00000143889	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12622920	0.94[EUR][1000 genomes]
rs13402042	0.81[EUR][1000 genomes]
rs17022893	0.82[AMR][1000 genomes]
rs58563643	0.81[AMR][1000 genomes]
rs7578342	1.00[EUR][1000 genomes]
rs7581419	0.81[AMR][1000 genomes]

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	nsv916059	chr2:38332341-39119398	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	143 gene(s)	inside rSNPs	diseases
2	nsv9646	chr2:38358311-39082189	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
3	nsv873881	chr2:38745624-38877636	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv581482	chr2:38799820-38858669	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv581483	chr2:38799820-38862223	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv581484	chr2:38799820-38874177	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:38775800-38821800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:38779000-38818200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:38779400-38821800	Weak transcription	Right Ventricle	heart
4	chr2:38781200-38827600	Weak transcription	Esophagus	oesophagus
5	chr2:38782400-38819000	Strong transcription	Fetal Thymus	thymus
6	chr2:38783800-38827800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:38785000-38827600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:38786000-38827600	Weak transcription	Colonic Mucosa	Colon
9	chr2:38786400-38818800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:38786600-38819000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:38798000-38818000	Weak transcription	Stomach Mucosa	stomach
12	chr2:38798000-38827600	Weak transcription	Spleen	Spleen
13	chr2:38798200-38820600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:38798200-38821800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr2:38798200-38827600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr2:38798600-38816400	Weak transcription	Brain Germinal Matrix	brain
17	chr2:38798800-38817000	Weak transcription	Brain Anterior Caudate	brain
18	chr2:38798800-38822000	Weak transcription	NHEK	skin
19	chr2:38799600-38817200	Weak transcription	Brain Substantia Nigra	brain
20	chr2:38799800-38827800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr2:38800000-38817800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr2:38800000-38818600	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr2:38800600-38816600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:38802800-38819000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr2:38805200-38826400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr2:38807200-38819000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:38808200-38824400	Weak transcription	Hela-S3	cervix
28	chr2:38808400-38820400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:38808800-38817200	Weak transcription	Placenta	Placenta
30	chr2:38808800-38817800	Weak transcription	Stomach Smooth Muscle	stomach
31	chr2:38808800-38819000	Strong transcription	Dnd41	blood
32	chr2:38808800-38821800	Weak transcription	HMEC	breast
33	chr2:38808800-38825200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr2:38808800-38825400	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr2:38808800-38827000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr2:38808800-38827400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr2:38808800-38827400	Weak transcription	Pancreas	Pancrea
38	chr2:38809000-38819600	Weak transcription	Brain Hippocampus Middle	brain
39	chr2:38809000-38824200	Weak transcription	Liver	Liver
40	chr2:38809000-38825600	Weak transcription	Brain Cingulate Gyrus	brain
41	chr2:38809200-38817600	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr2:38809200-38817800	Weak transcription	Brain Angular Gyrus	brain
43	chr2:38809200-38818000	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr2:38809400-38817200	Weak transcription	HSMMtube	muscle
45	chr2:38809400-38825800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr2:38809600-38827400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:38809800-38817800	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr2:38810000-38827600	Weak transcription	Fetal Muscle Trunk	muscle
49	chr2:38811400-38817800	Weak transcription	Right Atrium	heart
50	chr2:38811600-38819600	Weak transcription	NH-A	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links