Variant report

Variant	rs36073436
Chromosome Location	chr5:178252896-178252897
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031206	chr5:178149292-178283614	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv537973	chr5:178149292-178283614	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv883218	chr5:178219855-178349391	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv968861	chr5:178251700-178275142	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv600453	chr5:178252366-178259787	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178236800-178255800	Weak transcription	K562	blood
2	chr5:178252200-178253200	Enhancers	H9 Cell Line	embryonic stem cell
3	chr5:178252400-178253200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:178252400-178253400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr5:178252400-178254000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr5:178252400-178254600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr5:178252400-178255000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:178252600-178253000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr5:178252600-178253200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:178252600-178254200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr5:178252600-178254400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr5:178252600-178254400	Enhancers	HMEC	breast
13	chr5:178252600-178254600	Enhancers	NHEK	skin
14	chr5:178252600-178255000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:178252800-178253400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr5:178252800-178254000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr5:178252800-178254400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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