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

TagContent
EnhancerAtlas ID
HS055-00675 
Organism
Homo sapiens 
Tissue/cell
FT33 
Coordinate
chr1:202002980-202005400 
Target genes
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_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_57376chr1:202004143-202004423VACO_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
AACACTCCGT GAGGGCATGG CATTTTGCCT GCTTTGCTCA CAATGTGTAT CCCACTGAAG 60
ACATCCAATA AACAATTTAT CGAATAAATG AATGCATCTA CCTGATACCT CATCAAGAAA 120
TTGATGACCA CTAATTATCA TCTTTGAACC TCTGATTGGT GACCTCTGGC AAGGCTGAGG 180
ACCTTTAGCT CTAATCAATG GGCAAAAGGT TGACCTCTTT GCTACTGATT GGCTTTTCCT 240
TTTCATTATA CCCTTGGGCT GGATGGGGAA GCTGTGTGAA TCAACGCTTC ATAAGCCTTC 300
CTCTCTGAGA ACTAGGGCTT CCAAGGAATT GGATATGAAA AGGCAGAGAG GAAGGAGGAG 360
GATATGAGAT GCCAGACGGG GGAGGGTGGG GGGGACAGGT CCCAGAAGAG GTCAGCTGGG 420
ACCCAGGCAG GATGGCATTG TGGCTGCGGG TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC 480
CTCAGTCAGC CTTGACTGCT GGGTAATCCG TGGTAAGTAC CCACTGCTCC TGCCTCAGCT 540
TCCCCACCTC TCACATGTGG TTGATCCTCA CAGCCATCTC TTGGGGTTGT TCTGAAGATG 600
AAATGAGATC ATCTATGTAA GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC 660
GTATGGTCTG TCCTTATTTG GGGAATGGGG GTGGAAGGCG CCCAGCAGGG CATGGGGCGT 720
GGTATGGCAG AGCCAGGACT AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG 780
ATTTCCCATG TTCTCACCAT CTACAGAGTC ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC 840
CAAGTGGCCC TCACACTAGG TGGAGGAGCC CTCACAGATC TCTTTCCTTC AGCCTGCCGT 900
TCTTTCTGCA GCACCAGGGC CCTGGGACCA GCTGGTGGTT TCCACCAGAG CAGCCTCGGG 960
GTGAATTTAG TCAGGAATGT GCCCTCAGCT CAAGAGAACC CTCCCCAACC TTCCACTCCC 1020
CATACCCACC CCCGACCGCA GGTTCCCCAC CCACCCGTGG CCTGGCCAGC AGCAACCTCC 1080
ACTAGCTCGC TAGCTCAGTG ACGGTGACGT CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA 1140
CCCGCAAGTT TCACCTCTCC CTGGGGAGAC TGGATTACCT CACCCTGGGA GCAGAGTGAA 1200
TGATTAACCA GCTTCATCCT GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT AGGCCTACAG 1260
GGCAAGGGGC TGCATGGTCA CATACCCTAG TATGCGGGTT CACATACCCC AGCCGGGGCT 1320
GGGGTATGTG ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA TCTGCATCAC TGCTCACAAG 1380
TGTCATAAAA ATTTGTCTAC AGCATATATA AATATACATA TGACGTGGAA GGCTTCCGAT 1440
GGCAAATAAC ATTTTCCATT TTGCCTAAGC TTGGGTGGCT TTTTATTCAT CTATTGTTGT 1500
TTTAAGTACA CATTTCCATC TAAACTTAGA TGTATGTTTA GGCTGGCCGC GGTGGCTCAT 1560
TGCCTGTAAT CCCAGTACCT TTTAGGGGGT TGAGGCGGGT GGATCATTTG AGGCCAGCAG 1620
TTCAAGACCA GCCTGGCCAA CATGATGAAA CCTCGTCTCT ACTAAAAAAT ACAAAAATTA 1680
GCTGGGTGTG GTGGCAGGCG TCTGTAATCT CAGCTACTCG GGAGGCTGAG GCAGGAGAAT 1740
CACTTGAACC TGGGAGGCGG AGGCTGCAGT GAGCTGAGAT TGCACCATTG CACTCCAGCC 1800
TGGGCAACAG AGTGACATTC TGTCTCAAAA ACAAAAACAA AAACAAAACA AAAAAAATAA 1860
ACTTAGATGT ATATTTAAAA ATTGCTTTTT ACCCCTGAAG GTCTCAGCAT CCTACCTGCT 1920
CTATTCATTA GTGTTTAGAT TACCCATGAC ACCAGAAGGA CTTCCCAACC CAGAAAAAGA 1980
TCCAGGAGTT GATATAAAAT ATAGAACTAC TATAATATTA GCAACTTGGA GCAGCAAGTT 2040
CTTGACTTGG GAAAGTAGGA ATTCCTCTCA TTAAGAGATG TTTGCCCACA GGGAATGCTG 2100
CATAGAAAAG AATTTGGCTG GAACTCTTTT TTTCCACTAT GACTCCATTC ACACTTGAAT 2160
TGTTTCCTTT TACTTTTCTT TTTCTTTCTT TCTTTTTTTT TTTTTTTTTT GAGACAGAGT 2220
CTCGCTCTGT CACCCAGGCT GGAGTGCAGT GGCATGATCT CAGCTCACTG CAACCTCCGC 2280
CTCTCAGGTT TAAGCGATTC TCCTGCCTCA GCCTCCAGAG TAGCTGGGAT TACAGGCGCG 2340
CACCACCATG CCCGGCTAAT TTTCACATTT TTAATAGAGA TGGGGTTTTG CCATGTTGGC 2400
CAGGCTGGTT TTGAACTGCT 2420