Variant report

Variant	rs192474863
Chromosome Location	chr8:19536689-19536690
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:19534323..19537317-chr8:19613839..19616648,2	MCF-7	breast:
2	chr8:19535486..19538060-chr8:19539195..19541920,3	K562	blood:
3	chr8:19536477..19540083-chr8:19612902..19617470,5	MCF-7	breast:
4	chr8:19535666..19538060-chr8:19539355..19541920,2	K562	blood:

Variant related genes	Relation type
ENSG00000147408	Chromatin interaction

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

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	nsv949636	chr8:18957705-19664732	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv948861	chr8:19199688-19609029	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv949304	chr8:19199688-19625912	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats 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	11 gene(s)	inside rSNPs	diseases
4	nsv890625	chr8:19368697-19799641	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv890627	chr8:19389865-19561997	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1021575	chr8:19430653-19623452	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv1025271	chr8:19435147-19574969	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv6106	chr8:19499554-19544249	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1021731	chr8:19515149-19643313	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv890628	chr8:19527536-19540966	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv465602	chr8:19536015-19555398	Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv610757	chr8:19536015-19555398	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19520400-19539000	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr8:19520400-19539400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr8:19520400-19539600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr8:19520600-19538800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:19520600-19538800	Weak transcription	Esophagus	oesophagus
6	chr8:19520600-19538800	Weak transcription	Gastric	stomach
7	chr8:19523600-19538600	Weak transcription	Brain Anterior Caudate	brain
8	chr8:19523800-19540200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr8:19524200-19539000	Weak transcription	Ovary	ovary
10	chr8:19525400-19538800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr8:19528400-19538400	Weak transcription	Fetal Heart	heart
12	chr8:19528600-19538600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr8:19528600-19540200	Weak transcription	Spleen	Spleen
14	chr8:19528800-19538800	Weak transcription	Lung	lung
15	chr8:19530600-19538400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr8:19531000-19538400	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr8:19531200-19538600	Weak transcription	Brain Hippocampus Middle	brain
18	chr8:19532000-19539200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr8:19533400-19537800	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr8:19533400-19538000	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr8:19533600-19538600	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr8:19533800-19539000	Weak transcription	Thymus	Thymus
23	chr8:19534400-19536800	Enhancers	HUVEC	blood vessel
24	chr8:19534400-19539000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr8:19534600-19539200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr8:19534800-19538800	Weak transcription	Primary T cells from cord blood	blood
27	chr8:19535000-19537200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr8:19535200-19536800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr8:19535200-19537600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr8:19535200-19538600	Weak transcription	Left Ventricle	heart
31	chr8:19535200-19538600	Weak transcription	Right Atrium	heart
32	chr8:19535400-19537600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr8:19535400-19537600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr8:19535600-19537400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr8:19535600-19537600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr8:19535800-19537000	Flanking Active TSS	A549	lung
37	chr8:19535800-19537600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr8:19535800-19537800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr8:19536000-19537200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr8:19536000-19537400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr8:19536000-19537400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr8:19536000-19537600	Enhancers	Primary B cells from cord blood	blood
43	chr8:19536000-19537800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:19536000-19539200	Weak transcription	Fetal Lung	lung
45	chr8:19536200-19536800	Enhancers	HepG2	liver
46	chr8:19536200-19538000	Active TSS	Right Ventricle	heart
47	chr8:19536200-19539200	Weak transcription	NHLF	lung
48	chr8:19536200-19540800	Enhancers	Pancreas	Pancrea
49	chr8:19536400-19536800	Enhancers	Hela-S3	cervix
50	chr8:19536400-19536800	Enhancers	NH-A	brain

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