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

TagContent
EnhancerAtlas ID
HS095-11056 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr16:16115290-16116620 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17264736chr1616116556hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr16:16115586-16115598AAACAAACAAAC-6.32
NFE2L1MA0089.2chr16:16116061-16116076CGTGCTGAGTCACTG-6.01
Nfe2l2MA0150.2chr16:16116063-16116078TGCTGAGTCACTGAG-6.6
RUNX1MA0002.2chr16:16116281-16116292GTCTGTGGTTT+6.62
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_13655chr16:16113960-16117852CD34_Primary_RO01536
SE_26926chr16:16114478-16117838Esophagus
SE_32168chr16:16115386-16118019Gastric
SE_44900chr16:16115308-16116788NHLF
SE_47158chr16:16111262-16124112Panc1
SE_48435chr16:16114024-16117178Psoas_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr161611558516116553
Number: 1             
IDChromosomeStartEnd
GH16I016018chr161611251216117921
Enhancer Sequence
AGGCCAGGTG TGGTGGCTTA CACCTATAAA CCCAGCACTT TGGGAGGCCG AGGCAGGTAG 60
ATCACCTGAG ATCAGGAGTT TGAGACCAGC CTGACCAACA TGGTGAAATC CCATCTCTAC 120
TAAAAATACA AAAATTAGCT GGGCATGGTG TTGAGCACCT GTGATCCCTG CTATTTAGGA 180
GGCAGAGGCA GGAGAATTGC TTGTGCCCGG GAGGCGGAGG TTGCAGTGAG CTGAGATCGC 240
TCCAGTCTGG GCAACAGACT GAGACCCTGT CTCAAACAAA CAACGAACAA ATGAACAAAC 300
AAACAAACAA AATAACCACA TAACTACCTA GCAACGTAGC CTAGCAATTG AGATGGGGGC 360
AAGGAAGGGT AGGAACCAGG TCCTGTGAGA ATCAGCTAGA CTTGTGGCTT TGGGCTCGGT 420
GCTCTTCCTT TGGGGACGTC AGCAGCCCCT TCTTGAAAAC GGGTTGCAAC TCGATTTGTT 480
GTTGGCTTCA CCTCCTCTCT CTGTCCCAGA CCTGAGCCCT GTGATCTGGG GAGGAGGACA 540
ACGGGACAAC CTGTTTGCTT GTTTTCCCAT CACTCTCAGG GATTGAATCA CAGTGGAGCC 600
AGGAAGATGG GGAGAGTCCA GGCTTGCTGC TCTCCCATCC TCAGAGCAGC AGCAGGCCAT 660
CCATCACCTG TCGCCTGTCC TCAGAGTGAT CAGCCAAGGC CTGGGGCGGC TGGGGTCAGG 720
TCAGGCAGGG CGTGGGTGGG AGCTGGCAGG GCTGGCTCCT CCAGGCCACT TCGTGCTGAG 780
TCACTGAGTC GGCCAATCCT CCCCAGCTGG CCCTGCTCCC ACTCCATGAC TCAGATGTCT 840
ATTCCAGCCC TGGCTGCTTG GTGGGGCTCC TCCCATCTGT CCTTCTGGCT CTGGGGCTGC 900
CGAGGCTTTT GGGAGCCTGG GCAGGGCTGA CCAAGACTGC CAGAGCTCCG GCCGGTCCCC 960
AGTCTCCTGC CTTTTTTCTC ATTGGCACTG AGTCTGTGGT TTAGGTTTGG GGGAGGAGGG 1020
TCTTGTAGAT AAGGGGATCA AGGCCAAAGG AGATCATTTA TTAGGTCCCA GCTGAAAGCA 1080
GAGGTCCTTG GACCAGTTGG AATGCTCGAC ATCCCCCGGA AGCTTGCTAG AAATGCTGGG 1140
TCTCAGGCCT CATCCCAGAC CTACCAAGTC AAACTCATTT TAACAAGATC TCCAGGTGGT 1200
TCAGGGTTGC AAATCACTGG TTTGGAACAT TCAGTGAAAG CTACTCAGCT CGTTTGCAGT 1260
AAGAGGTATT TTTAGTCCTG TCTGTATAAT ATGTAATATT TTCCCCCCAG CATTTTACTA 1320
TGAACATTCT 1330