Variant report

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(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:76444677..76445883-chr11:76549434..76550433,4	K562	blood:
2	chr11:76445344..76446073-chr11:76801899..76802836,2	K562	blood:
3	chr11:76445248..76448071-chr11:76628717..76631883,4	MCF-7	breast:
4	chr11:76444321..76446462-chr11:76517342..76520030,2	K562	blood:
5	chr11:76444662..76445640-chr11:76629853..76630608,2	MCF-7	breast:
6	chr11:76444642..76445671-chr11:76509955..76510846,7	K562	blood:
7	chr11:76443783..76447678-chr11:76493146..76497317,7	MCF-7	breast:
8	chr11:76444583..76446069-chr11:76756756..76757887,9	MCF-7	breast:
9	chr11:76443601..76445826-chr11:76571953..76574772,2	K562	blood:
10	chr11:76445009..76450493-chr11:76452594..76458852,7	K562	blood:
11	chr11:76444941..76447137-chr11:76494986..76497317,3	K562	blood:
12	chr11:76444817..76447367-chr11:76477489..76481018,3	MCF-7	breast:
13	chr11:76444941..76446826-chr11:76495647..76497317,2	K562	blood:

No data

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	esv1810781	chr11:76311021-76464814	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	esv1850014	chr11:76384895-76464814	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv976471	chr11:76435262-76459660	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv430404	chr11:76436952-76462852	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	esv2311913	chr11:76445186-76445654	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76433400-76456400	Weak transcription	Right Atrium	heart
2	chr11:76441400-76450200	Weak transcription	Liver	Liver
3	chr11:76445000-76446800	Enhancers	K562	blood
4	chr11:76445200-76446200	Enhancers	Fetal Intestine Small	intestine
5	chr11:76445200-76446400	Enhancers	Fetal Muscle Trunk	muscle
6	chr11:76445200-76446600	Enhancers	Colon Smooth Muscle	Colon
7	chr11:76445200-76446800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr11:76445200-76446800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr11:76445200-76448000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr11:76445200-76448800	Enhancers	A549	lung
11	chr11:76445400-76445800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:76445400-76448000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr11:76445600-76446000	Weak transcription	Fetal Thymus	thymus
14	chr11:76445600-76446200	Enhancers	Fetal Intestine Large	intestine
15	chr11:76445600-76446800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr11:76445600-76446800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr11:76445600-76447200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr11:76445600-76447200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr11:76445600-76447400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:76445600-76447800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr11:76445600-76448200	Enhancers	Placenta	Placenta
22	chr11:76445600-76450600	Enhancers	Fetal Heart	heart

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