Variant report

Variant	rs139955260
Chromosome Location	chr8:63215940-63215941
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019143	chr8:63142202-63390820	Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2757277	chr8:63156123-63260182	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv2759621	chr8:63156123-63260182	Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv818632	chr8:63208699-63222881	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
5	esv2761215	chr8:63212769-63229146	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	nsv611445	chr8:63214002-63227321	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3515684	chr8:63214098-63226396	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv2443694	chr8:63214138-63226350	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	nsv6225	chr8:63214240-63262285	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
10	esv3515683	chr8:63214648-63226246	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv2484852	chr8:63214789-63225986	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	nsv8356	chr8:63215158-63225678	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3515682	chr8:63215200-63225306	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3479356	chr8:63215208-63225350	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv2159853	chr8:63215215-63225390	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3515679	chr8:63215239-63225378	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3479358	chr8:63215256-63225324	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3515680	chr8:63215271-63225335	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3479355	chr8:63215273-63225361	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv3479357	chr8:63215294-63225342	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
21	nsv515094	chr8:63215334-63225046	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv3479359	chr8:63215336-63225232	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
23	esv18522	chr8:63215345-63225085	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
24	esv3515681	chr8:63215346-63225233	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
25	nsv499495	chr8:63215349-63225231	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv3479360	chr8:63215350-63225231	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv3515686	chr8:63215350-63225231	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv3692989	chr8:63215615-63222881	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
29	nsv517136	chr8:63215615-63222881	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
30	nsv465699	chr8:63215615-63222881	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
31	nsv465700	chr8:63215615-63222881	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
32	nsv611446	chr8:63215615-63222881	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
33	nsv818634	chr8:63215615-63222881	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
34	esv2421340	chr8:63215615-63224085	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
35	nsv818635	chr8:63215615-63245683	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63212400-63216200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr8:63214400-63216200	Enhancers	Fetal Brain Female	brain
3	chr8:63215000-63216000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:63215200-63216000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr8:63215200-63216000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr8:63215400-63216000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr8:63215600-63216000	Enhancers	ES-WA7 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links