EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS089-00431 
Organism
Homo sapiens 
Tissue/cell
Hela 
Coordinate
chr1:44404920-44406020 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11210937chr144405563hg19
TF binding sites/motifs
Number: 36             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:44404947-44404965GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr1:44404955-44404973GGAGGGAGGGGAGGGAGG+6.09
EWSR1-FLI1MA0149.1chr1:44404926-44404944GAGGGGAGGGAAGGAAGG+6.22
EWSR1-FLI1MA0149.1chr1:44404921-44404939GGAAGGAGGGGAGGGAAG+6.41
EWSR1-FLI1MA0149.1chr1:44405011-44405029GGAAGGAAGGAAGGGGAA+6.42
EWSR1-FLI1MA0149.1chr1:44404968-44404986GGAGGGAAGGAGGGGAGG+6.59
EWSR1-FLI1MA0149.1chr1:44404938-44404956GGAAGGAGGGGAGGGAGG+7.21
EWSR1-FLI1MA0149.1chr1:44404972-44404990GGAAGGAGGGGAGGGAGG+7.21
EWSR1-FLI1MA0149.1chr1:44405003-44405021GGAGAGAGGGAAGGAAGG+7.21
EWSR1-FLI1MA0149.1chr1:44404964-44404982GGAGGGAGGGAAGGAGGG+7.36
EWSR1-FLI1MA0149.1chr1:44404934-44404952GGAAGGAAGGAGGGGAGG+7.79
EWSR1-FLI1MA0149.1chr1:44405007-44405025AGAGGGAAGGAAGGAAGG+7.85
EWSR1-FLI1MA0149.1chr1:44404930-44404948GGAGGGAAGGAAGGAGGG+8.34
ZNF263MA0528.1chr1:44405343-44405364TCCTCTTCCTCTCTCTGCCTC-6.08
ZNF263MA0528.1chr1:44404936-44404957AAGGAAGGAGGGGAGGGAGGG+6.13
ZNF263MA0528.1chr1:44405016-44405037GAAGGAAGGGGAAAGAGAGAG+6.36
ZNF263MA0528.1chr1:44404932-44404953AGGGAAGGAAGGAGGGGAGGG+6.41
ZNF263MA0528.1chr1:44404970-44404991AGGGAAGGAGGGGAGGGAGGG+6.55
ZNF263MA0528.1chr1:44405000-44405021GAGGGAGAGAGGGAAGGAAGG+6.79
ZNF263MA0528.1chr1:44404978-44404999AGGGGAGGGAGGGAGGGGGAG+6.84
ZNF263MA0528.1chr1:44404965-44404986GAGGGAGGGAAGGAGGGGAGG+6.8
ZNF263MA0528.1chr1:44404969-44404990GAGGGAAGGAGGGGAGGGAGG+7.05
ZNF263MA0528.1chr1:44404982-44405003GAGGGAGGGAGGGGGAGGGAG+7.15
ZNF263MA0528.1chr1:44404927-44404948AGGGGAGGGAAGGAAGGAGGG+7.19
ZNF263MA0528.1chr1:44404956-44404977GAGGGAGGGGAGGGAGGGAAG+7.21
ZNF263MA0528.1chr1:44404986-44405007GAGGGAGGGGGAGGGAGGGAG+7.32
ZNF263MA0528.1chr1:44404948-44404969GAGGGAGGGAGGGAGGGGAGG+7.43
ZNF263MA0528.1chr1:44404922-44404943GAAGGAGGGGAGGGAAGGAAG+7.47
ZNF263MA0528.1chr1:44404944-44404965AGGGGAGGGAGGGAGGGAGGG+7.54
ZNF263MA0528.1chr1:44404996-44405017GAGGGAGGGAGAGAGGGAAGG+7.62
ZNF263MA0528.1chr1:44404935-44404956GAAGGAAGGAGGGGAGGGAGG+7.86
ZNF263MA0528.1chr1:44404961-44404982AGGGGAGGGAGGGAAGGAGGG+7.86
ZNF263MA0528.1chr1:44404992-44405013GGGGGAGGGAGGGAGAGAGGG+7.92
ZNF263MA0528.1chr1:44404952-44404973GAGGGAGGGAGGGGAGGGAGG+8.26
ZNF263MA0528.1chr1:44404939-44404960GAAGGAGGGGAGGGAGGGAGG+8.67
ZNF263MA0528.1chr1:44404973-44404994GAAGGAGGGGAGGGAGGGAGG+8.67
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14440509444405400
Number: 1             
IDChromosomeStartEnd
GH01I043938chr14440389744404946
Enhancer Sequence
GGGAAGGAGG GGAGGGAAGG AAGGAGGGGA GGGAGGGAGG GAGGGGAGGG AGGGAAGGAG 60
GGGAGGGAGG GAGGGGGAGG GAGGGAGAGA GGGAAGGAAG GAAGGGGAAA GAGAGAGAGA 120
AAGCAAGAAG CAAGCAAGAA AGAAAAGGTT GTTTTCCCCA AAGGAAACAG GCTGCAGAGC 180
TGTACCTCTG TTTACCACAT AGTAGCTATA ACCTGTCACC AGGTGGCACA TTGTAGCTCC 240
TGGGGCCACA GGTGACTCTG GTCAATACTA AAGCCAAAGG CCATTTAGTC CTTTGAAGTC 300
TCAGAAGCAT TCGATAGTGT CAGTCCTCCT TGAAAACCTG TCTTCCCGTG ACTCTCTTGG 360
TCCAATACTC TCCGGGTTCT CCTTCCACTC CTCCAGAGGC TTGTTCTCAG ACGACTTCTG 420
AGTTCCTCTT CCTCTCTCTG CCTCTCATGT TCCTCAGAGC TCTGATACCG ACTCTCTCTC 480
CTCTTCCCAT TCTACTCTCT CCCTGAGCAG CACTGTCTAC TCCCGTGGTT TCAGTTACCA 540
CCTCCATGCT AACCATGCTC ACATTTTATC TCCAGCCTAG AACATTCACC TGAGCCCCAA 600
GTCTGTAATT CCAATACCTC TATCTGTATA TCCTGGGAGA CATCAAGCTT AACATATCCA 660
TACTGGATGT CTTCCGTTTC CTCCTTCAGA TCTGCTGTCC ACCCTTCTCC AGCCTGCTCT 720
GCTCCTCACA TCAATGAGCT TCCCTGCTGT CCAGCTTCCA GACCCTCCCC AGTGTTCCCT 780
GCTCAGTGAG TGCACCAACC TCATCCAGTG ACACAGCCAG AAACTTGGGC AATCTCCTAG 840
GCTCCTTAAG CTCTGTCATG TCCCTTAAGC ATTGGTCACC AAATCCTTAG ATCCTGCAGA 900
TCCATCCCCT TTCCCTATCC CCAGTGCTAT TCTGCTGAAG CCTTCATAAT TTTTTGGATG 960
GTTTATTCCT CATCCTCCTA CCTGGTCTCA CTGTCTCCAG TCACAACTCC CTCCAACCAT 1020
TCTCAGCGCT GCAGCCAGAT AAGTTGCCTT CTCTTCATAT TAACCGAGCA TGAACTGTCG 1080
TGCACTGGGC TAGTTTCAGG 1100