Variant report

Variant	rs77904936
Chromosome Location	chr2:173007088-173007089
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:43 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv528818	chr2:173001058-173013373	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv435726	chr2:173001856-173008530	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3459871	chr2:173002306-173009204	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3524175	chr2:173002605-173009327	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3451254	chr2:173003006-173008754	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3386960	chr2:173003556-173008504	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3459869	chr2:173003788-173007782	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3358596	chr2:173004076-173007618	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv989435	chr2:173004125-173009154	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3459868	chr2:173004129-173007602	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3377911	chr2:173004140-173007571	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv3524172	chr2:173004180-173007539	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3524176	chr2:173004180-173007539	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	esv3459870	chr2:173004185-173007559	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	nsv511824	chr2:173004215-173007569	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv3459872	chr2:173004249-173007496	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
17	esv10774	chr2:173004360-173007310	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	nsv821494	chr2:173004360-173007310	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
19	esv1792573	chr2:173004862-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
20	esv1794743	chr2:173004862-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
21	esv1794775	chr2:173004862-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
22	esv1799053	chr2:173004862-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
23	esv1801155	chr2:173004862-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
24	esv1819033	chr2:173004862-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
25	esv1826132	chr2:173004862-173007203	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv1832763	chr2:173004862-173007203	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv1834134	chr2:173004862-173007203	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv1834525	chr2:173004862-173007203	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
29	esv1834698	chr2:173004862-173007203	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
30	esv1838685	chr2:173004862-173007203	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
31	esv1840004	chr2:173004862-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
32	nsv583641	chr2:173004964-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
33	nsv583650	chr2:173005293-173007203	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
34	nsv583654	chr2:173005671-173007203	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
35	nsv583658	chr2:173005728-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
36	esv3340009	chr2:173005731-173008579	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
37	nsv583659	chr2:173005800-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
38	nsv583660	chr2:173005966-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
39	nsv511160	chr2:173006114-173008793	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
40	esv1010793	chr2:173006172-173007310	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
41	esv14611	chr2:173006172-173007310	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
42	nsv583661	chr2:173006618-173007203	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
43	nsv583662	chr2:173006890-173007203	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173002200-173012600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:173004400-173007200	Weak transcription	Fetal Brain Male	brain
3	chr2:173006600-173012600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:173006800-173010600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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