EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS183-02022 
Organism
Homo sapiens 
Tissue/cell
T47D-MTVL 
Coordinate
chr17:29890830-29892280 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs62063930chr1729891429hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CDX2MA0465.1chr17:29891789-29891800TTTTATGGCTC-6.14
SP2MA0516.2chr17:29891896-29891913CAGGGGGCAGGGCTTAC-6.08
SREBF2MA0596.1chr17:29891993-29892003ATCACCCCAT-6.02
ZNF263MA0528.1chr17:29892229-29892250GGAGGATGGGAGGGCTGGGGG+6.11
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_00097chr17:29884943-29903384Adipose_Nuclei
SE_27382chr17:29891001-29891598Esophagus
SE_27382chr17:29891625-29893307Esophagus
SE_33988chr17:29890922-29894815HCC1954
SE_37031chr17:29890703-29893725HSMMtube
SE_44284chr17:29890720-29893125NHDF-Ad
SE_45954chr17:29890579-29902407Osteoblasts
SE_47701chr17:29891335-29892414Pancreas
SE_55681chr17:29890501-29900599u87
SE_65467chr17:29890939-29893536Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr172989213429892258
chr172989119529891341
Number: 1             
IDChromosomeStartEnd
GH17I031563chr172989092229896350
Enhancer Sequence
AACTATATGC GTGTCGTCAG GCCCAAGGGC CTCTTCCATC CTTGTCAAGG GGAGTGCTAA 60
CCTTCTCTCC TTTCATACAA TCCAGCTCTC TTATTTTGAA TCTGCGTGTA TATACATGTT 120
GGTTGAGACC GGTGCAGAGT GATTGAGACT CGGGCTTGTG GGTCTGGTAG GTTCGAGGAC 180
TAACTCCATC GCTTGGGAGC ATGTGGCCTT GGGCAAGTTA CTTAATCCAC TGGGAACAGG 240
GGTATCGTAA CCATCAGATG GGGATACTGT CTGGGATTCC CATCCCCTAT ATGGGTCTCA 300
ATCCTCTCAG TTTCTGTGGT CTAACAACTA TGTGCCAGGG ACTGGGCCAG GCAGAGGCTG 360
GGGTATCCGT TAGTAAGATG GGCACGGTCC CTCGCTGCCT GCTCTGATTT TTGCCCCAGC 420
TCTGAGAGCA GATTAATGGT ATTGTAAGTC CTCATTGTAT GGTTGAAGTC GAGACTCAGG 480
GGAAGAGACC CTCCCAGAAT CTCCCAGCTT GCCTCGGTAC CATAGGAGCA GGACCCCCAG 540
GCTTCCAGGT GCAGCCTCCC AGGTCGGAAG CCAGCAAGCT GGGGCTGTAG AACAGGAGGT 600
GGCTGGGCCT GGATTCGCTG GCACTGAGTC CTTAAAGGAA CCCTGGGTAG CAGATGTGGC 660
CGCCTTGTAC ATCTGCTCAG CAGTGCATCA CTCCTAAAGG CCCAAAGACT CGTCCGGTCC 720
TGACACTGAG CACGTTTCAG AAAAGGTCCC AGGAAAGACA TTTGAATTGC CACAGCTGCT 780
CAAGGCTTGC TCCCTCACTC ATGCTGTGGG CAAACTAAAC ATCCTCTAGT GGGACCAGGC 840
AAGCAGGGGA CAAAATGGAA TGGGGGTGCG GGGGAGGAGA AAATAATTTG ATATTCCAAA 900
AAATGCTGCA GAGTAATCAT TTTGGGGGTG AAAATCAGAA TTTCTTGGGA CTTAGACTTT 960
TTTATGGCTC AGTGGTGTTT TTCTTTAGAA TTTTGGACTG GAGGTAGGGA TAGACCATAA 1020
TCTTTTCAGC ACCCAAGAGC CTTCAGCAGG CCTCACTGGC TCTGGGCAGG GGGCAGGGCT 1080
TACAGGACCC AGAGCAGGTG ACATCTTACC CACTGTGGAT ACTTCCTCCC TCCTCCCTTT 1140
GGCACGGTCT GAGGAATTTT GAAATCACCC CATAGCCAGA CCCCTTGCAT TTGCTGCCCA 1200
GGAGAACCGG GCAGGGAGGT GCCATGCGGA AAGTCCCGCT GCCTGATTTT CCTCTGAGCT 1260
CATCACTGCA GCCTGAGAGC CCCCTTCTCT GTCAAGTGGG TGACTGAACT GAATACACCA 1320
GACCCCCCTT GGCATTCTTC TAAGATCCTA AGGAGGAGGA GCTGAGGAAG GCACGGGGTG 1380
GAGCCTGGGG CTGTGGTTTG GAGGATGGGA GGGCTGGGGG AGGGATTCAG AGATTGCAGC 1440
TGGGAAATTT 1450