Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TBL1XR1	chr11:17279638-17279920	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:17278678..17280712-chr11:17283886..17286306,2	K562	blood:
2	chr11:17276902..17279261-chr11:17279604..17281506,2	K562	blood:
3	chr11:17229468..17231636-chr11:17279187..17282001,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:3)

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	nsv467711	chr11:17027555-17320797	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv553568	chr11:17027555-17320797	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv469762	chr11:17170690-17320691	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv482905	chr11:17170690-17320691	Strong transcription Weak transcription Enhancers 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	24 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	chr11:17278000-17280400	Enhancers	A549	lung
2	chr11:17278600-17280200	Enhancers	K562	blood
3	chr11:17278600-17280600	Enhancers	Stomach Mucosa	stomach
4	chr11:17278800-17280000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr11:17278800-17280000	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr11:17278800-17281000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:17278800-17288800	Weak transcription	Placenta	Placenta
8	chr11:17279000-17280000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr11:17279000-17280000	Enhancers	Hela-S3	cervix
10	chr11:17279000-17281000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:17279000-17281000	Weak transcription	NHEK	skin
12	chr11:17279000-17281200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:17279000-17284600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr11:17279000-17284600	Weak transcription	NHLF	lung
15	chr11:17279000-17284800	Weak transcription	HMEC	breast
16	chr11:17279200-17284600	Weak transcription	Osteobl	bone
17	chr11:17279400-17280400	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr11:17279600-17280600	Enhancers	HepG2	liver
19	chr11:17279800-17284400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:17279800-17285000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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