Variant report

Variant	rs112869342
Chromosome Location	chr8:59078788-59078789
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:59077992..59080616-chr8:59081477..59083573,2	MCF-7	breast:

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	esv2589647	chr8:59078095-59079512	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv512049	chr8:59078180-59078955	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv6064	chr8:59078198-59079062	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2299885	chr8:59078277-59078980	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3510687	chr8:59078359-59078898	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3479310	chr8:59078364-59078889	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3510686	chr8:59078367-59078874	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3510689	chr8:59078376-59078841	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3510684	chr8:59078378-59078822	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3479307	chr8:59078390-59078851	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3510683	chr8:59078395-59078839	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv4205	chr8:59078397-59078938	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3479306	chr8:59078398-59078810	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3510688	chr8:59078409-59078833	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3337699	chr8:59078415-59078809	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3479309	chr8:59078438-59078794	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3510690	chr8:59078452-59078789	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv1008809	chr8:59078453-59078788	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3479311	chr8:59078453-59078801	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3510691	chr8:59078453-59078801	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv1644581	chr8:59078788-59078789	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59068400-59085000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:59074800-59083200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr8:59075000-59082000	Weak transcription	Fetal Muscle Leg	muscle
4	chr8:59075400-59080800	Weak transcription	HepG2	liver
5	chr8:59075600-59079000	Weak transcription	GM12878-XiMat	blood
6	chr8:59075800-59079600	Weak transcription	Primary monocytes fromperipheralblood	blood

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