Variant report

Variant	rs147402374
Chromosome Location	chr17:16389916-16389917
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:16388573..16391176-chr17:16394299..16396980,2	K562	blood:
2	chr17:16374663..16376189-chr17:16388387..16389969,2	MCF-7	breast:
3	chr17:16281117..16284005-chr17:16388491..16391199,2	MCF-7	breast:
4	chr17:16371050..16373790-chr17:16387962..16391461,3	MCF-7	breast:
5	chr17:16366570..16369549-chr17:16387763..16390396,2	MCF-7	breast:
6	chr17:16388461..16390561-chr17:16439173..16440871,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000181350	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
3	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
4	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS 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 miRNA target site	164 gene(s)	inside rSNPs	diseases
5	nsv1063764	chr17:16171649-16662914	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Enhancers Active TSS 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	120 gene(s)	inside rSNPs	diseases
6	nsv1061463	chr17:16245878-16490691	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
7	nsv543216	chr17:16245878-16490691	Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
8	nsv1065254	chr17:16252880-16389930	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
9	nsv428668	chr17:16265210-16455285	Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	89 gene(s)	inside rSNPs	diseases
10	nsv1063941	chr17:16357086-16424098	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	nsv574487	chr17:16389498-16395496	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
12	esv1794587	chr17:16389498-16395680	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
13	nsv1058448	chr17:16389870-16926287	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16375200-16390400	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr17:16381000-16390000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr17:16381200-16392600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr17:16385800-16392200	Genic enhancers	Fetal Intestine Small	intestine
5	chr17:16386200-16392600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr17:16387400-16390400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr17:16387600-16390600	Flanking Active TSS	Fetal Brain Female	brain
8	chr17:16387600-16390800	Enhancers	Fetal Brain Male	brain
9	chr17:16387600-16392800	Enhancers	Fetal Lung	lung
10	chr17:16387600-16393000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr17:16387600-16393000	Enhancers	Placenta	Placenta
12	chr17:16387800-16390600	Enhancers	Brain Substantia Nigra	brain
13	chr17:16387800-16392400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr17:16387800-16392600	Enhancers	Fetal Heart	heart
15	chr17:16387800-16393000	Enhancers	Ovary	ovary
16	chr17:16388000-16390600	Enhancers	Fetal Stomach	stomach
17	chr17:16388200-16390000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr17:16388200-16390000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr17:16388200-16390200	Weak transcription	K562	blood
20	chr17:16388200-16390400	Enhancers	H9 Cell Line	embryonic stem cell
21	chr17:16388200-16391000	Enhancers	Fetal Muscle Trunk	muscle
22	chr17:16388200-16392200	Enhancers	Spleen	Spleen
23	chr17:16388200-16392600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr17:16388200-16392800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr17:16388400-16390000	Enhancers	Brain Cingulate Gyrus	brain
26	chr17:16388400-16391200	Enhancers	Stomach Mucosa	stomach
27	chr17:16388400-16392000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr17:16388400-16392800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr17:16388600-16390000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr17:16388600-16390600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr17:16388600-16390600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr17:16388600-16392400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr17:16388800-16392400	Enhancers	Gastric	stomach
34	chr17:16389000-16390200	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr17:16389000-16390400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr17:16389000-16390400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr17:16389000-16390400	Enhancers	Liver	Liver
38	chr17:16389000-16390600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr17:16389000-16390600	Enhancers	Lung	lung
40	chr17:16389000-16391000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr17:16389000-16392800	Enhancers	Pancreas	Pancrea
42	chr17:16389200-16390200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr17:16389200-16390200	Flanking Active TSS	Stomach Smooth Muscle	stomach
44	chr17:16389200-16390200	Flanking Active TSS	HUVEC	blood vessel
45	chr17:16389200-16390400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr17:16389200-16390400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr17:16389200-16390400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
48	chr17:16389200-16390400	Enhancers	Fetal Thymus	thymus
49	chr17:16389200-16390600	Flanking Active TSS	Rectal Smooth Muscle	rectum
50	chr17:16389200-16390800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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