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

TagContent
EnhancerAtlas ID
HS095-07777 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr12:108698980-108700390 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1878022chr12108699032hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr12:108699909-108699924TGCCCTCTGACCTCT-7.55
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_01739chr12:108695822-108703047Aorta
SE_20399chr12:108696650-108702723CD56
SE_37376chr12:108695174-108703146HSMMtube
SE_42751chr12:108695023-108702737Lung
SE_46420chr12:108696207-108703824Osteoblasts
SE_52020chr12:108698184-108702317Skeletal_Muscle_Myoblast
SE_63774chr12:108698134-108702428HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12108699402108699607
chr12108700100108700298
Number: 1             
IDChromosomeStartEnd
GH12I108301chr12108695555108703251
Enhancer Sequence
AACTGTGCCT GGGACTTCCA TAACTTCTGC CTCAGTGTGA TCCACATAGA CCGTTCCATA 60
GATTTGCAAA TAGGGACTCA GAGAGGTGAA GTGACTAGTC CAGATTCACA CAGCCTTTAA 120
GCATCAGCTC GGGATTTGAA CCAAGGACTT TTTGACCCCA AAGCACAAGA TCACAGCCTC 180
AACCAGCAGC TGAAATGTAA TGAGGCGGGC CAGTCACCAC TCTTGCCCTC AAAAATGTCT 240
CTCCTGAGCA GCATACCAGC CTCCCCCTGG CCTGGACGAC TGTAGGTGCT GATGTCTTTG 300
CCTGCTGCCT TCTGGGCCAG TCCATTCACC AGATCTCCTA CCCTCCAGGG CAGAGAGAAG 360
GGGCCTCTCA TCTCCCAAGG ATGGCTCCAG AGACACCTCC AGATCCCTGT ATCCCCAGGC 420
TCTGACAGAC TCGGGAACCT GGAAACCACA CAGTGTCTGC AGATGTTCCA GCCACAGGCC 480
TGGCTGCCAG CCCCAGGACA GAATTAGCTC CGTGTCAGGA GAGAATTTCC TCCCTGGTCC 540
CACGCCCACA TGTGGGAGCT CGCACTGAGT CACTGCAGCA GAGCAGAGCG GCACGGGCTG 600
CCTAACAGAC TGTCCCATTT TCTTTCGGGT TTGGAAGGGG CCACGACGGA GCTTAGGACT 660
CCATAAGAAT GGGCAAAAAC AAGGAGCTTA TGCCCCTGAA CCCAGACAGC CCACCTGCTT 720
AGAGGCCAGG AAAAGCAGCT GATGAGCTCA CCGACTCAGG GAGACCCCCC CACCCAAAAT 780
ATTCACGCCA CTGCCTGGCA TCCTCCCATT AGAACACTAC TCCTTGAGCC TTAAAAGCGT 840
TTCCTTCCTC TCCGGGGATC TCTGTCTCCA GATCCCTGTC TGTTCTGTGC CCTACAGGCT 900
GACCTGCTTG AAAATCTCAA TAGGCTGTTT GCCCTCTGAC CTCTGGTTTG ATCCACAACT 960
GCAGGCGTGG AGCGTGCGGT TGGGTACAAA CCCTCCAGCT CCCTCCTTGT CAGAGGTGTG 1020
CGGGTTGGCC ACAGCCACAC TCCTTGGGTG CCTTAACTAC TTCCTGCTCT AGCCCCTCAG 1080
TCTAGGAACA GTGAGTTCTC GCCTTCACTG GACCCGGAGC GTGGTAGGGA TCCCTTGTAC 1140
TGTCTACCCT TTTGTCAGTC CTCCCCTGAC TAAGTTCTCG TTAATCACCT CATTTGAGTG 1200
GGTTGTCCAT CTCCTGCCAA CACTCTGACT CAGAAACCAG ACTCTCCACA CTTTCCCCTC 1260
CCTCCCTACC CACACATCTA TCAACAAGTT CTTCCCATTT TGTCCTCCCA ACAACTCACA 1320
GCTGTGAGCA TCACCTCTGC TTACCTATGT GGCTACCAGG GGCTCCTAAC TGGTTAGAAA 1380
CCTATCTACC TAGTACACAG ACCATTTTAT 1410