EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-02780 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr1:202002740-202005590 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CREB1MA0018.3chr1:202004082-202004094GGTGACGTCAGC+6.14
CREB1MA0018.3chr1:202004082-202004094GGTGACGTCAGC-6.14
Foxq1MA0040.1chr1:202003046-202003057AATAAACAATT-6.02
IRF1MA0050.2chr1:202005141-202005162GTTTCCTTTTACTTTTCTTTT+6.23
IRF1MA0050.2chr1:202005162-202005183TCTTTCTTTCTTTTTTTTTTT+6.25
NFAT5MA0606.1chr1:202004430-202004440ATTTTCCATT+6.02
NFATC1MA0624.1chr1:202004430-202004440ATTTTCCATT+6.02
NFATC3MA0625.1chr1:202004430-202004440ATTTTCCATT+6.02
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_23058chr1:202003070-202004639Colon_Crypt_1
SE_23723chr1:202003133-202004433Colon_Crypt_2
SE_24689chr1:202003019-202005179Colon_Crypt_3
SE_25977chr1:202003098-202005224Duodenum_Smooth_Muscle
SE_26730chr1:202003201-202004852Esophagus
SE_27624chr1:202002753-202007729Fetal_Intestine
SE_28545chr1:202002635-202005490Fetal_Intestine_Large
SE_31432chr1:202003030-202004833Gastric
SE_31432chr1:202005212-202005566Gastric
SE_33417chr1:202002752-202008344H2171
SE_33792chr1:202002877-202005297HCC1954
SE_34304chr1:202003057-202005125HCT-116
SE_34741chr1:202002989-202005297HeLa
SE_41626chr1:202003359-202004353LNCaP
SE_43434chr1:202002760-202004009MCF-7
SE_43434chr1:202004034-202004676MCF-7
SE_50066chr1:202002922-202004883Sigmoid_Colon
SE_52354chr1:202003018-202004869Small_Intestine
SE_56834chr1:202002917-202004651VACO_400
SE_57376chr1:202003233-202004124VACO_503
SE_57945chr1:202003251-202004112VACO_9m
SE_57945chr1:202004146-202004634VACO_9m
SE_65333chr1:202002930-202005541Pancreatic_islets
SE_67013chr1:202002752-202008344H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1202003606202003949
Number: 1             
IDChromosomeStartEnd
GH01I202033chr1202002815202007566
Enhancer Sequence
GCACATGTAT ACCTGTGAAA CAAACCTGCA TGTTGTGCAC ATGTACCCTA TAACTTAAAG 60
TATAATAATA ATAAAAAAAA ACACAAAAAT AATTGTAACC CATTGCCCAC CCTAGCCCTG 120
CCCGCCTTCC TATCTTCTTT CTTGGTTTTA TTTTTCTCCA TAGCATTTAT CATGCTCAGA 180
CACACAAAAT ATTTATCTAT TTTTGCTGTT TGTAATTGTC TTTCTCCCCC CACTAAAATG 240
AACACTCCGT GAGGGCATGG CATTTTGCCT GCTTTGCTCA CAATGTGTAT CCCACTGAAG 300
ACATCCAATA AACAATTTAT CGAATAAATG AATGCATCTA CCTGATACCT CATCAAGAAA 360
TTGATGACCA CTAATTATCA TCTTTGAACC TCTGATTGGT GACCTCTGGC AAGGCTGAGG 420
ACCTTTAGCT CTAATCAATG GGCAAAAGGT TGACCTCTTT GCTACTGATT GGCTTTTCCT 480
TTTCATTATA CCCTTGGGCT GGATGGGGAA GCTGTGTGAA TCAACGCTTC ATAAGCCTTC 540
CTCTCTGAGA ACTAGGGCTT CCAAGGAATT GGATATGAAA AGGCAGAGAG GAAGGAGGAG 600
GATATGAGAT GCCAGACGGG GGAGGGTGGG GGGGACAGGT CCCAGAAGAG GTCAGCTGGG 660
ACCCAGGCAG GATGGCATTG TGGCTGCGGG TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC 720
CTCAGTCAGC CTTGACTGCT GGGTAATCCG TGGTAAGTAC CCACTGCTCC TGCCTCAGCT 780
TCCCCACCTC TCACATGTGG TTGATCCTCA CAGCCATCTC TTGGGGTTGT TCTGAAGATG 840
AAATGAGATC ATCTATGTAA GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC 900
GTATGGTCTG TCCTTATTTG GGGAATGGGG GTGGAAGGCG CCCAGCAGGG CATGGGGCGT 960
GGTATGGCAG AGCCAGGACT AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG 1020
ATTTCCCATG TTCTCACCAT CTACAGAGTC ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC 1080
CAAGTGGCCC TCACACTAGG TGGAGGAGCC CTCACAGATC TCTTTCCTTC AGCCTGCCGT 1140
TCTTTCTGCA GCACCAGGGC CCTGGGACCA GCTGGTGGTT TCCACCAGAG CAGCCTCGGG 1200
GTGAATTTAG TCAGGAATGT GCCCTCAGCT CAAGAGAACC CTCCCCAACC TTCCACTCCC 1260
CATACCCACC CCCGACCGCA GGTTCCCCAC CCACCCGTGG CCTGGCCAGC AGCAACCTCC 1320
ACTAGCTCGC TAGCTCAGTG ACGGTGACGT CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA 1380
CCCGCAAGTT TCACCTCTCC CTGGGGAGAC TGGATTACCT CACCCTGGGA GCAGAGTGAA 1440
TGATTAACCA GCTTCATCCT GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT AGGCCTACAG 1500
GGCAAGGGGC TGCATGGTCA CATACCCTAG TATGCGGGTT CACATACCCC AGCCGGGGCT 1560
GGGGTATGTG ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA TCTGCATCAC TGCTCACAAG 1620
TGTCATAAAA ATTTGTCTAC AGCATATATA AATATACATA TGACGTGGAA GGCTTCCGAT 1680
GGCAAATAAC ATTTTCCATT TTGCCTAAGC TTGGGTGGCT TTTTATTCAT CTATTGTTGT 1740
TTTAAGTACA CATTTCCATC TAAACTTAGA TGTATGTTTA GGCTGGCCGC GGTGGCTCAT 1800
TGCCTGTAAT CCCAGTACCT TTTAGGGGGT TGAGGCGGGT GGATCATTTG AGGCCAGCAG 1860
TTCAAGACCA GCCTGGCCAA CATGATGAAA CCTCGTCTCT ACTAAAAAAT ACAAAAATTA 1920
GCTGGGTGTG GTGGCAGGCG TCTGTAATCT CAGCTACTCG GGAGGCTGAG GCAGGAGAAT 1980
CACTTGAACC TGGGAGGCGG AGGCTGCAGT GAGCTGAGAT TGCACCATTG CACTCCAGCC 2040
TGGGCAACAG AGTGACATTC TGTCTCAAAA ACAAAAACAA AAACAAAACA AAAAAAATAA 2100
ACTTAGATGT ATATTTAAAA ATTGCTTTTT ACCCCTGAAG GTCTCAGCAT CCTACCTGCT 2160
CTATTCATTA GTGTTTAGAT TACCCATGAC ACCAGAAGGA CTTCCCAACC CAGAAAAAGA 2220
TCCAGGAGTT GATATAAAAT ATAGAACTAC TATAATATTA GCAACTTGGA GCAGCAAGTT 2280
CTTGACTTGG GAAAGTAGGA ATTCCTCTCA TTAAGAGATG TTTGCCCACA GGGAATGCTG 2340
CATAGAAAAG AATTTGGCTG GAACTCTTTT TTTCCACTAT GACTCCATTC ACACTTGAAT 2400
TGTTTCCTTT TACTTTTCTT TTTCTTTCTT TCTTTTTTTT TTTTTTTTTT GAGACAGAGT 2460
CTCGCTCTGT CACCCAGGCT GGAGTGCAGT GGCATGATCT CAGCTCACTG CAACCTCCGC 2520
CTCTCAGGTT TAAGCGATTC TCCTGCCTCA GCCTCCAGAG TAGCTGGGAT TACAGGCGCG 2580
CACCACCATG CCCGGCTAAT TTTCACATTT TTAATAGAGA TGGGGTTTTG CCATGTTGGC 2640
CAGGCTGGTT TTGAACTGCT GACTTCAACT GATCCACCTG TCTGGGTCTC CCAAAGTGCT 2700
GGGATTACAG GCGTGAACAC AGCATGTTTC CGTTTTCAAA ATAAGATATG TCCTAATTGC 2760
TGTGAATTTT TAAAAGAGAA TTATTTTCCA TGACACATTC TGTTTTCAGA TGTACTGACT 2820
TTAGGAGTTG GTAAATAGTC CTCTAGCAAT 2850