Variant report

Variant	rs74008003
Chromosome Location	chr15:35201531-35201532
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:35198651..35201621-chr15:35206696..35208281,2	K562	blood:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs13910	1.00[AMR][1000 genomes]
rs59300844	0.95[AFR][1000 genomes]
rs61741130	1.00[AMR][1000 genomes]
rs74008006	0.95[AFR][1000 genomes]
rs74009743	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74009747	1.00[AMR][1000 genomes]
rs74009748	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350109	chr15:34668106-35534229	Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv522411	chr15:34953986-35462981	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv457106	chr15:35049787-35227613	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv569153	chr15:35049787-35227613	Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	esv2761865	chr15:35101678-35271639	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv832967	chr15:35110102-35267906	Strong transcription Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv904071	chr15:35150897-35250771	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv904072	chr15:35150897-35259376	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv569154	chr15:35165366-35259376	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	7 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	chr15:35140400-35221600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:35185200-35205200	Weak transcription	Stomach Mucosa	stomach
3	chr15:35186000-35204200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:35186000-35206400	Weak transcription	Right Ventricle	heart
5	chr15:35186000-35206600	Weak transcription	Small Intestine	intestine
6	chr15:35186000-35212400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr15:35186000-35212600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr15:35186000-35213000	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr15:35186000-35220000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr15:35186000-35220000	Weak transcription	Pancreas	Pancrea
11	chr15:35186000-35223200	Weak transcription	Gastric	stomach
12	chr15:35186000-35232000	Weak transcription	Fetal Brain Male	brain
13	chr15:35186200-35202200	Weak transcription	NHEK	skin
14	chr15:35186200-35212000	Strong transcription	Primary B cells from peripheral blood	blood
15	chr15:35186200-35212400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr15:35186200-35212400	Strong transcription	Liver	Liver
17	chr15:35186400-35205400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr15:35186400-35238800	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr15:35186600-35204000	Weak transcription	NHLF	lung
20	chr15:35186600-35206000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr15:35186600-35212200	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr15:35186600-35212200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr15:35186600-35212400	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr15:35187200-35204000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr15:35187200-35204200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr15:35187200-35212000	Strong transcription	HUES64 Cell Line	embryonic stem cell
27	chr15:35187400-35212000	Strong transcription	Adipose Nuclei	Adipose
28	chr15:35187800-35204200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr15:35191400-35212800	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr15:35192000-35212200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr15:35192200-35204200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr15:35192200-35211200	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr15:35192200-35212200	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr15:35192200-35212400	Strong transcription	Placenta	Placenta
35	chr15:35192400-35212000	Strong transcription	Duodenum Mucosa	Duodenum
36	chr15:35192400-35212400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr15:35192600-35212000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr15:35192600-35212400	Strong transcription	A549	lung
39	chr15:35193200-35204200	Weak transcription	Psoas Muscle	Psoas
40	chr15:35193200-35206600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr15:35193400-35204000	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr15:35193400-35205200	Weak transcription	Stomach Smooth Muscle	stomach
43	chr15:35193400-35205400	Weak transcription	Osteobl	bone
44	chr15:35193800-35206400	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr15:35194200-35207600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr15:35194800-35205200	Strong transcription	HSMM	muscle
47	chr15:35195600-35208400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr15:35195800-35205800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr15:35196600-35207800	Strong transcription	Fetal Intestine Large	intestine
50	chr15:35196600-35211000	Strong transcription	Brain Inferior Temporal Lobe	brain

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