Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:129445172..129447751-chr7:129449224..129452364,3	K562	blood:
2	chr7:129445172..129447751-chr7:129449224..129452042,3	K562	blood:
3	chr7:129443362..129446037-chr7:129458801..129461329,2	K562	blood:

rSNPs within LD-proxies of this variant (count:9)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv14232	chr7:129379923-129445465	Flanking Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	365 gene(s)	inside rSNPs	diseases
2	esv1843969	chr7:129403541-129446598	Bivalent Enhancer Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	365 gene(s)	inside rSNPs	diseases
3	esv33085	chr7:129438848-129446659	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv819865	chr7:129443525-129445605	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:129441200-129445400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:129442600-129447600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:129443600-129445600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:129443600-129445600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:129443600-129445600	Enhancers	Gastric	stomach
6	chr7:129443800-129445600	Enhancers	Placenta	Placenta
7	chr7:129444000-129445400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr7:129444200-129445600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:129444600-129445400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:129444600-129445600	Enhancers	Fetal Heart	heart
11	chr7:129444600-129445600	Enhancers	Right Ventricle	heart
12	chr7:129444600-129445600	Enhancers	Hela-S3	cervix
13	chr7:129444800-129445600	Enhancers	Left Ventricle	heart
14	chr7:129445000-129445400	Enhancers	Duodenum Mucosa	Duodenum
15	chr7:129445000-129445400	Enhancers	Stomach Mucosa	stomach
16	chr7:129445000-129445600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr7:129445000-129445600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:129445000-129445600	Enhancers	K562	blood
19	chr7:129445200-129445600	Enhancers	H1 Cell Line	embryonic stem cell
20	chr7:129445200-129445600	Enhancers	Fetal Muscle Trunk	muscle
21	chr7:129445200-129445600	Enhancers	Fetal Muscle Leg	muscle
22	chr7:129445200-129464600	Weak transcription	Right Atrium	heart

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