Variant report

No.	Distal block	Cell Line	Cell type
1	chr14:31708924..31710880-chr14:31720802..31723577,2	K562	blood:
2	chr14:31697845..31699989-chr14:31707051..31710155,3	MCF-7	breast:
3	chr14:31705909..31709311-chr14:31711142..31713834,3	K562	blood:
4	chr14:31701418..31703156-chr14:31707210..31709221,2	K562	blood:
5	chr14:31705909..31710425-chr14:31710546..31713834,4	K562	blood:

rSNPs within LD-proxies of this variant (count:11)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901587	chr14:31501505-31752664	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1050054	chr14:31501703-31733642	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	esv2830427	chr14:31639110-32000034	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31703000-31710200	Weak transcription	Fetal Heart	heart
2	chr14:31707800-31709000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:31707800-31710600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr14:31707800-31710600	Weak transcription	Colon Smooth Muscle	Colon
5	chr14:31707800-31710600	Weak transcription	Stomach Mucosa	stomach
6	chr14:31707800-31711000	Weak transcription	Esophagus	oesophagus
7	chr14:31707800-31711000	Weak transcription	Spleen	Spleen
8	chr14:31707800-31712800	Weak transcription	Lung	lung
9	chr14:31707800-31713400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:31707800-31730800	Weak transcription	Pancreas	Pancrea
11	chr14:31708600-31709000	Enhancers	Primary B cells from peripheral blood	blood
12	chr14:31708600-31709000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr14:31708600-31709000	Flanking Active TSS	K562	blood
14	chr14:31708600-31709200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr14:31708600-31710000	Enhancers	GM12878-XiMat	blood
16	chr14:31708800-31709000	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr14:31708800-31709200	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr14:31708800-31709400	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr14:31708800-31709800	Enhancers	HepG2	liver
20	chr14:31708800-31710600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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