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

TagContent
EnhancerAtlas ID
HS026-13488 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr17:4384020-4385110 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr17:4384890-4384905AGAGGGCAGAGGGCA+6.62
ZEB1MA0103.3chr17:4384160-4384171CCCACCTGCCC+6.14
ZNF263MA0528.1chr17:4384335-4384356GGGTGAGGAGGGTGAGGGAGG+6.58
ZNF263MA0528.1chr17:4384329-4384350GGAGCAGGGTGAGGAGGGTGA+6.72
ZNF263MA0528.1chr17:4384338-4384359TGAGGAGGGTGAGGGAGGGGA+7.18
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_23583chr17:4382378-4385214Colon_Crypt_1
SE_24329chr17:4382476-4385188Colon_Crypt_2
SE_26970chr17:4384372-4385197Esophagus
SE_28097chr17:4378603-4387608Fetal_Intestine
SE_29102chr17:4378472-4387704Fetal_Intestine_Large
SE_31567chr17:4382469-4385277Gastric
SE_42277chr17:4383361-4385251Lung
SE_53037chr17:4381447-4385287Small_Intestine
SE_53662chr17:4384026-4385141Spleen
SE_57545chr17:4382493-4385202VACO_503
SE_57914chr17:4384151-4385051VACO_9m
SE_65581chr17:4383216-4387811Pancreatic_islets
Number: 1             
IDChromosomeStartEnd
GH17I004475chr1743784694387600
Enhancer Sequence
TTTGGGGAGC TGCCCAGGGA GCCGGCTGGA CAGGAACCAG CCCACCTCAG GGCTCCCTGT 60
GGCCCTTCCT TGGCTTGGAG GCCTCCAGCC ACAATGCTTT GCACCACCAT CCCAGAGCCT 120
CCCGCCCCCT TCCCTGCCTT CCCACCTGCC CGGAGCCCCG TGGCCAAAGA TGCCTTTTGG 180
CCTTCGGGGA TCAGAGCTGA GCAATCCTTG TAGCCCCTAT AGTTCGGTTC CTCCATGTTG 240
CTGCTTCCTC CCTGTAAAGG CAGGTGGTGG GGGAGCCGTT CTGTGCAGTG GAGGGGCAGA 300
TGCCAGCTTG GAGCAGGGTG AGGAGGGTGA GGGAGGGGAA GCAGGACACC GAGGGTAGAC 360
AATTCCCTTG AGGAGCTGAG CTGACAGGAG CAAAGGGCAT GGTAGCTGGA GTTGGCAGAA 420
GATCCCAGGA AGCTGGCATT GCTTTTCAAG AGGGGAGGAC AGAACAGCCT CCAGGGAGCA 480
GAGAGGGGCA AGCAGGAGGA GAGAGGGGGC CATGTTTGAG GGTGAGCTGG GGGTGGAATC 540
CAGCACTGGG GGAGGAAGTG GCCTCCCAGC AGAGCAGGGG CAGGAAGTGT GTGGGGACAG 600
GGTCTGTGGC AGGAAGTAGA GGAAGGTCCC CTTTGCCGGC CGGCACTGGC TCCTGAGACA 660
GGAGATCGGC TTCTCTTTCA GCAGGGGCCC AGGGAGGGAG GAGGCCTTAG GGTGTGTGTG 720
AACAGGGTCC ACAGAACAAG GGAGCAGGAA GCTAAGGGCA GGGCACGTTC ACGTGAACAG 780
CTTTGGGCGG CCAAGAAAGC CACGAGGAGC TGATAGGAAA ATGGGTGGAA ACTGCAGGTG 840
TCTGGGTGGT TGGAGCCTGT GGGTTAGGTC AGAGGGCAGA GGGCAGCAGA GCCCAGGCTC 900
GAGGACTCTG CAGCAGCCCA TCTGCTCCCA CTCCCAGCCT GGCTCCTCAC TAGCTGTGTG 960
ACCCTGGCCA AGTGACTGAA CCTCTCTGGG TCTTGGTTTG CTCACCTGTC CAGTAGGTAG 1020
AGCGGTGGCA ACCACCATTG ACACCCCAGG CTATAAGGAT AGAATGAACT CACACCTGCG 1080
TCCTGCAGAT 1090