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

TagContent
EnhancerAtlas ID
HS108-14117 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr15:90834700-90835910 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF13MA0657.1chr15:90835075-90835093AGGCCACGCCCCTATTCT+6.56
KLF14MA0740.1chr15:90835076-90835090GGCCACGCCCCTAT+6.29
Klf12MA0742.1chr15:90835076-90835091GGCCACGCCCCTATT+6.69
SP1MA0079.4chr15:90835074-90835089AAGGCCACGCCCCTA+6.36
SP4MA0685.1chr15:90835017-90835034CTGGCCACGCCTCCTTT+6.35
SP4MA0685.1chr15:90835074-90835091AAGGCCACGCCCCTATT+6.73
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr159083495090835243
chr159083561090835814
chr159083527590835331
Enhancer Sequence
AAGGTAATAC TGGTAATTAT TGTACTCCAT TTGAAGATGA AAAATATAGG CCAAAATTAT 60
AGACCTTGCA TAGAAGCTGG ATAATGGAGA CAGCTCTGGA GGAACACGTA GATACACACA 120
CACAGACACA CATATATATA AAGAATACAC ACATACATTT TTTAAAGTTT ATTTTTTACA 180
GTTTTAAAGG TTTTAAAGCA AAAGCCGGCC CCTCCCCTCT GAGTGGGCGG CCCCTCCCTC 240
TCTCTGAGTG GTCGGGTACA GCGGTTGCAT GGGCAGCTTT CCTTGTGAAC CACAGGTCCT 300
TCTGGACACG GTGCTACCTG GCCACGCCTC CTTTCCCTTT CATATTTCTC ATTGACCAAT 360
GGGCTTGGAG CATTAAGGCC ACGCCCCTAT TCTGCATTCT AGTGGGGCCC CGGTTATGCC 420
TCTTCTGGCT CAGTTGCACA GCTGCCTGGT AGGTGACTGG AGGCATTCAT CAGTGCTCAC 480
TGGGATTTCA CTGATGTGGC CCAACCCCGC CTCCCTCCAC ACCCCATGAT GTCAGAAAAA 540
ACACGACAGG GCAAATGGGC CGCAGCCAGG AAAAAGGTAA AACGCACCAG GTCATGGCCC 600
CCAACCCAGC CACAGATCCC CTCCGACAAC AAGACCGTTG CCGGAGTCCA TACCACCCCT 660
GAGGCACACT GGACTGGGCC CCCCAACCCC AGCCCTCCTC CCTAGCCCGC CAGGCCTTTG 720
TTTCCCCACC TGTAAAATGG GGCAGTGTAG CCCTCACATG AAATGGTACT TCTAAGGCAC 780
CTGTGAGCCG GAGCCCTGCT CTGATGGCTG TGGGAGAGAG GGGATGATTT TTCTAACCTC 840
CCTCCACCCT TCCCAGTGCT ATGGGAGGCA GACACCAAGT TCTGGGGTCT CCAGTTGCAG 900
CGGGTGGCTG CTGATTGCTT CTCTCTGTCC AGAACGAGAA CAAGAGCGCA CTGCAGTTGG 960
AGCAGCAAGT AAAGGAGCTG CAGGAGAAGC TGGGCTAGCT GAAGGGGACG GTAACCTCCG 1020
ACCCGTCCAA GAAGGTCTGG GAGGCGGGCA CCAGCCTCTG GGGAGGGGAG GTGCCAGGCC 1080
AGAGGCAGCT GCAGCCTGGG GGCAGGTGAC CCCAGCACCC TCCAGGGCAG TCCTATGACT 1140
GTTTCTTGCT TCCTGCCCTC TGACTTTTAG AGGTGGGTAG CCCTGGCTCC TCCCAGGTCT 1200
GGACATCATC 1210