Variant report

Variant	rs76582654
Chromosome Location	chr15:58596844-58596845
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:58343646..58346573-chr15:58595833..58597683,2	K562	blood:
2	chr15:58595612..58601278-chr15:58601529..58605992,7	K562	blood:
3	chr15:58596834..58598473-chr15:58598758..58600301,2	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	nsv1047246	chr15:58375607-58707158	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv833024	chr15:58447459-58621963	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1051058	chr15:58519922-59092530	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv542401	chr15:58519922-59092530	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv529717	chr15:58519923-58756814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1042201	chr15:58520746-58780710	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv569598	chr15:58552606-58852463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	nsv904266	chr15:58580921-58689187	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	esv2460369	chr15:58595796-58597424	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv8982	chr15:58596230-58597108	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv2279007	chr15:58596311-58597025	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3311266	chr15:58596388-58596922	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3520556	chr15:58596400-58596898	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3520554	chr15:58596404-58596928	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv5355	chr15:58596406-58596939	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3520555	chr15:58596419-58596869	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3520553	chr15:58596423-58596854	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3311267	chr15:58596432-58596894	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3520558	chr15:58596442-58596870	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3311265	chr15:58596444-58596845	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv3520557	chr15:58596464-58596870	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58587400-58598800	Weak transcription	Fetal Kidney	kidney
2	chr15:58590200-58602400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:58592000-58598600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr15:58593400-58598400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr15:58595000-58598800	Weak transcription	Adipose Nuclei	Adipose
6	chr15:58595000-58598800	Weak transcription	Fetal Muscle Leg	muscle
7	chr15:58595200-58598600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr15:58595400-58597200	Weak transcription	Liver	Liver
9	chr15:58595400-58598800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr15:58595600-58599000	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr15:58595800-58598400	Weak transcription	Fetal Thymus	thymus
12	chr15:58595800-58598600	Weak transcription	Primary T cells from cord blood	blood
13	chr15:58595800-58598800	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr15:58595800-58599000	Weak transcription	Thymus	Thymus
15	chr15:58595800-58601800	Weak transcription	K562	blood
16	chr15:58595800-58605000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr15:58596000-58599200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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