Variant report

Variant	rs706035
Chromosome Location	chr7:16734425-16734426
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:16726055..16728607-chr7:16734001..16737874,4	K562	blood:
2	chr7:16685700..16688239-chr7:16731845..16734495,2	K562	blood:
3	chr7:16687442..16689722-chr7:16734234..16736098,2	MCF-7	breast:
4	chr7:16729664..16732572-chr7:16733703..16735363,2	MCF-7	breast:
5	chr7:16684775..16687164-chr7:16733474..16737702,4	MCF-7	breast:
6	chr7:16684062..16686546-chr7:16733471..16737128,4	MCF-7	breast:
7	chr7:16733508..16735059-chr7:16737961..16740377,2	K562	blood:

Variant related genes	Relation type
ENSG00000136261	Chromatin interaction
ENSG00000106524	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10228088	1.00[CHD][hapmap]
rs10239553	0.91[LWK][hapmap];0.85[YRI][hapmap]
rs10243402	0.85[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv1028125	chr7:16529160-16847225	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv830912	chr7:16623196-16791974	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv1024059	chr7:16639432-16836425	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv464397	chr7:16709708-16782767	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv606338	chr7:16709708-16782767	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv887760	chr7:16714974-16776257	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16697800-16736400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:16697800-16736400	Weak transcription	Fetal Brain Male	brain
3	chr7:16701200-16736200	Weak transcription	Pancreas	Pancrea
4	chr7:16701200-16736600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:16701800-16752800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:16704200-16737600	Weak transcription	Aorta	Aorta
7	chr7:16708200-16737400	Weak transcription	Brain Substantia Nigra	brain
8	chr7:16708400-16736200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr7:16708800-16747800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:16710200-16752400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr7:16712400-16737400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:16714000-16737200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr7:16714000-16741800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:16714000-16747200	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr7:16714000-16748400	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr7:16715400-16736200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr7:16715800-16734600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr7:16716600-16735400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:16719200-16741800	Strong transcription	A549	lung
20	chr7:16719200-16746800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr7:16720200-16735000	Weak transcription	Fetal Kidney	kidney
22	chr7:16720200-16736600	Weak transcription	Fetal Brain Female	brain
23	chr7:16720800-16748800	Strong transcription	Placenta	Placenta
24	chr7:16722000-16737600	Weak transcription	Psoas Muscle	Psoas
25	chr7:16722200-16736400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr7:16722800-16736800	Weak transcription	Brain Angular Gyrus	brain
27	chr7:16723400-16736200	Weak transcription	Brain Hippocampus Middle	brain
28	chr7:16724000-16735400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr7:16724000-16735600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr7:16724600-16747200	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr7:16725000-16736800	Strong transcription	HUVEC	blood vessel
32	chr7:16725200-16739000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr7:16725200-16749000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr7:16725400-16734600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr7:16725400-16746000	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr7:16725400-16749400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:16726200-16735600	Weak transcription	HSMMtube	muscle
38	chr7:16726200-16736400	Weak transcription	Brain Anterior Caudate	brain
39	chr7:16726800-16740600	Strong transcription	Fetal Intestine Large	intestine
40	chr7:16726800-16750600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:16727600-16742400	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr7:16727600-16748800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr7:16727800-16749000	Strong transcription	Dnd41	blood
44	chr7:16728400-16746400	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr7:16728600-16742400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr7:16728600-16747400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr7:16729000-16736600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:16729000-16741000	Strong transcription	HMEC	breast
49	chr7:16729000-16743000	Strong transcription	Fetal Thymus	thymus
50	chr7:16729000-16746800	Strong transcription	Primary monocytes fromperipheralblood	blood

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