EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS122-01162 
Organism
Homo sapiens 
Tissue/cell
LoVo 
Coordinate
chr1:202002630-202005560 
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
AAAAAAAAAA AAAACAGCAA CAAAAGGAGA GTGGGAGGCT GGGGGAGGGA TAGCATTAGG 60
AGAAATACCT AATGTAAATG ACGAGTTGAT GGGTGCAGCA AACCAACATG GCACATGTAT 120
ACCTGTGAAA CAAACCTGCA TGTTGTGCAC ATGTACCCTA TAACTTAAAG TATAATAATA 180
ATAAAAAAAA ACACAAAAAT AATTGTAACC CATTGCCCAC CCTAGCCCTG CCCGCCTTCC 240
TATCTTCTTT CTTGGTTTTA TTTTTCTCCA TAGCATTTAT CATGCTCAGA CACACAAAAT 300
ATTTATCTAT TTTTGCTGTT TGTAATTGTC TTTCTCCCCC CACTAAAATG AACACTCCGT 360
GAGGGCATGG CATTTTGCCT GCTTTGCTCA CAATGTGTAT CCCACTGAAG ACATCCAATA 420
AACAATTTAT CGAATAAATG AATGCATCTA CCTGATACCT CATCAAGAAA TTGATGACCA 480
CTAATTATCA TCTTTGAACC TCTGATTGGT GACCTCTGGC AAGGCTGAGG ACCTTTAGCT 540
CTAATCAATG GGCAAAAGGT TGACCTCTTT GCTACTGATT GGCTTTTCCT TTTCATTATA 600
CCCTTGGGCT GGATGGGGAA GCTGTGTGAA TCAACGCTTC ATAAGCCTTC CTCTCTGAGA 660
ACTAGGGCTT CCAAGGAATT GGATATGAAA AGGCAGAGAG GAAGGAGGAG GATATGAGAT 720
GCCAGACGGG GGAGGGTGGG GGGGACAGGT CCCAGAAGAG GTCAGCTGGG ACCCAGGCAG 780
GATGGCATTG TGGCTGCGGG TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC 840
CTTGACTGCT GGGTAATCCG TGGTAAGTAC CCACTGCTCC TGCCTCAGCT TCCCCACCTC 900
TCACATGTGG TTGATCCTCA CAGCCATCTC TTGGGGTTGT TCTGAAGATG AAATGAGATC 960
ATCTATGTAA GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC GTATGGTCTG 1020
TCCTTATTTG GGGAATGGGG GTGGAAGGCG CCCAGCAGGG CATGGGGCGT GGTATGGCAG 1080
AGCCAGGACT AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG ATTTCCCATG 1140
TTCTCACCAT CTACAGAGTC ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC 1200
TCACACTAGG TGGAGGAGCC CTCACAGATC TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA 1260
GCACCAGGGC CCTGGGACCA GCTGGTGGTT TCCACCAGAG CAGCCTCGGG GTGAATTTAG 1320
TCAGGAATGT GCCCTCAGCT CAAGAGAACC CTCCCCAACC TTCCACTCCC CATACCCACC 1380
CCCGACCGCA GGTTCCCCAC CCACCCGTGG CCTGGCCAGC AGCAACCTCC ACTAGCTCGC 1440
TAGCTCAGTG ACGGTGACGT CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT 1500
TCACCTCTCC CTGGGGAGAC TGGATTACCT CACCCTGGGA GCAGAGTGAA TGATTAACCA 1560
GCTTCATCCT GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT AGGCCTACAG GGCAAGGGGC 1620
TGCATGGTCA CATACCCTAG TATGCGGGTT CACATACCCC AGCCGGGGCT GGGGTATGTG 1680
ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA TCTGCATCAC TGCTCACAAG TGTCATAAAA 1740
ATTTGTCTAC AGCATATATA AATATACATA TGACGTGGAA GGCTTCCGAT GGCAAATAAC 1800
ATTTTCCATT TTGCCTAAGC TTGGGTGGCT TTTTATTCAT CTATTGTTGT TTTAAGTACA 1860
CATTTCCATC TAAACTTAGA TGTATGTTTA GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT 1920
CCCAGTACCT TTTAGGGGGT TGAGGCGGGT GGATCATTTG AGGCCAGCAG TTCAAGACCA 1980
GCCTGGCCAA CATGATGAAA CCTCGTCTCT ACTAAAAAAT ACAAAAATTA GCTGGGTGTG 2040
GTGGCAGGCG TCTGTAATCT CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CACTTGAACC 2100
TGGGAGGCGG AGGCTGCAGT GAGCTGAGAT TGCACCATTG CACTCCAGCC TGGGCAACAG 2160
AGTGACATTC TGTCTCAAAA ACAAAAACAA AAACAAAACA AAAAAAATAA ACTTAGATGT 2220
ATATTTAAAA ATTGCTTTTT ACCCCTGAAG GTCTCAGCAT CCTACCTGCT CTATTCATTA 2280
GTGTTTAGAT TACCCATGAC ACCAGAAGGA CTTCCCAACC CAGAAAAAGA TCCAGGAGTT 2340
GATATAAAAT ATAGAACTAC TATAATATTA GCAACTTGGA GCAGCAAGTT CTTGACTTGG 2400
GAAAGTAGGA ATTCCTCTCA TTAAGAGATG TTTGCCCACA GGGAATGCTG CATAGAAAAG 2460
AATTTGGCTG GAACTCTTTT TTTCCACTAT GACTCCATTC ACACTTGAAT TGTTTCCTTT 2520
TACTTTTCTT TTTCTTTCTT TCTTTTTTTT TTTTTTTTTT GAGACAGAGT CTCGCTCTGT 2580
CACCCAGGCT GGAGTGCAGT GGCATGATCT CAGCTCACTG CAACCTCCGC CTCTCAGGTT 2640
TAAGCGATTC TCCTGCCTCA GCCTCCAGAG TAGCTGGGAT TACAGGCGCG CACCACCATG 2700
CCCGGCTAAT TTTCACATTT TTAATAGAGA TGGGGTTTTG CCATGTTGGC CAGGCTGGTT 2760
TTGAACTGCT GACTTCAACT GATCCACCTG TCTGGGTCTC CCAAAGTGCT GGGATTACAG 2820
GCGTGAACAC AGCATGTTTC CGTTTTCAAA ATAAGATATG TCCTAATTGC TGTGAATTTT 2880
TAAAAGAGAA TTATTTTCCA TGACACATTC TGTTTTCAGA TGTACTGACT 2930