Variant report

Variant	rs578157278
Chromosome Location	chr2:209452040-209452041
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:209436667..209438687-chr2:209450893..209452499,2	K562	blood:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2493689	chr2:209451033-209452683	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3327660	chr2:209451057-209453055	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv2340327	chr2:209451536-209452239	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv6403	chr2:209451553-209452278	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3459956	chr2:209451596-209452126	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3525925	chr2:209451613-209452132	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3525927	chr2:209451630-209452154	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3525931	chr2:209451643-209452099	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3525932	chr2:209451647-209452081	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3459957	chr2:209451652-209452113	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv5250	chr2:209451660-209452115	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3525930	chr2:209451664-209452099	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3525928	chr2:209451675-209452093	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3366889	chr2:209451679-209452064	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3459958	chr2:209451679-209452115	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3459955	chr2:209451702-209452052	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3525926	chr2:209451717-209452045	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv213744	chr2:209451718-209452044	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3459959	chr2:209451718-209452059	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3525933	chr2:209451718-209452059	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv1448206	chr2:209451731-209452058	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209438800-209459400	Weak transcription	K562	blood
2	chr2:209449400-209458800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links