EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS175-02644 
Organism
Homo sapiens 
Tissue/cell
SK-N-MC 
Coordinate
chr1:202002900-202005600 
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: 25             
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_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
TAGCATTTAT CATGCTCAGA CACACAAAAT ATTTATCTAT TTTTGCTGTT TGTAATTGTC 60
TTTCTCCCCC CACTAAAATG AACACTCCGT GAGGGCATGG CATTTTGCCT GCTTTGCTCA 120
CAATGTGTAT CCCACTGAAG ACATCCAATA AACAATTTAT CGAATAAATG AATGCATCTA 180
CCTGATACCT CATCAAGAAA TTGATGACCA CTAATTATCA TCTTTGAACC TCTGATTGGT 240
GACCTCTGGC AAGGCTGAGG ACCTTTAGCT CTAATCAATG GGCAAAAGGT TGACCTCTTT 300
GCTACTGATT GGCTTTTCCT TTTCATTATA CCCTTGGGCT GGATGGGGAA GCTGTGTGAA 360
TCAACGCTTC ATAAGCCTTC CTCTCTGAGA ACTAGGGCTT CCAAGGAATT GGATATGAAA 420
AGGCAGAGAG GAAGGAGGAG GATATGAGAT GCCAGACGGG GGAGGGTGGG GGGGACAGGT 480
CCCAGAAGAG GTCAGCTGGG ACCCAGGCAG GATGGCATTG TGGCTGCGGG TGCCAGAGTC 540
AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC CTTGACTGCT GGGTAATCCG TGGTAAGTAC 600
CCACTGCTCC TGCCTCAGCT TCCCCACCTC TCACATGTGG TTGATCCTCA CAGCCATCTC 660
TTGGGGTTGT TCTGAAGATG AAATGAGATC ATCTATGTAA GAAGCTGGCA CTTAAAAGCA 720
CAGAGAGGGC ACCAAGGAAC GTATGGTCTG TCCTTATTTG GGGAATGGGG GTGGAAGGCG 780
CCCAGCAGGG CATGGGGCGT GGTATGGCAG AGCCAGGACT AAGGGTCTGT AGCCTCCTAA 840
ATCAGGGCTT TCTCCGCAGG ATTTCCCATG TTCTCACCAT CTACAGAGTC ACTCCCCTCC 900
ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC TCACACTAGG TGGAGGAGCC CTCACAGATC 960
TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA GCACCAGGGC CCTGGGACCA GCTGGTGGTT 1020
TCCACCAGAG CAGCCTCGGG GTGAATTTAG TCAGGAATGT GCCCTCAGCT CAAGAGAACC 1080
CTCCCCAACC TTCCACTCCC CATACCCACC CCCGACCGCA GGTTCCCCAC CCACCCGTGG 1140
CCTGGCCAGC AGCAACCTCC ACTAGCTCGC TAGCTCAGTG ACGGTGACGT CAGCCCTGCA 1200
GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT TCACCTCTCC CTGGGGAGAC TGGATTACCT 1260
CACCCTGGGA GCAGAGTGAA TGATTAACCA GCTTCATCCT GGAGGGCCTC AAAGGCCCGT 1320
CCTGGGGTGT AGGCCTACAG GGCAAGGGGC TGCATGGTCA CATACCCTAG TATGCGGGTT 1380
CACATACCCC AGCCGGGGCT GGGGTATGTG ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA 1440
TCTGCATCAC TGCTCACAAG TGTCATAAAA ATTTGTCTAC AGCATATATA AATATACATA 1500
TGACGTGGAA GGCTTCCGAT GGCAAATAAC ATTTTCCATT TTGCCTAAGC TTGGGTGGCT 1560
TTTTATTCAT CTATTGTTGT TTTAAGTACA CATTTCCATC TAAACTTAGA TGTATGTTTA 1620
GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT CCCAGTACCT TTTAGGGGGT TGAGGCGGGT 1680
GGATCATTTG AGGCCAGCAG TTCAAGACCA GCCTGGCCAA CATGATGAAA CCTCGTCTCT 1740
ACTAAAAAAT ACAAAAATTA GCTGGGTGTG GTGGCAGGCG TCTGTAATCT CAGCTACTCG 1800
GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGAGGCGG AGGCTGCAGT GAGCTGAGAT 1860
TGCACCATTG CACTCCAGCC TGGGCAACAG AGTGACATTC TGTCTCAAAA ACAAAAACAA 1920
AAACAAAACA AAAAAAATAA ACTTAGATGT ATATTTAAAA ATTGCTTTTT ACCCCTGAAG 1980
GTCTCAGCAT CCTACCTGCT CTATTCATTA GTGTTTAGAT TACCCATGAC ACCAGAAGGA 2040
CTTCCCAACC CAGAAAAAGA TCCAGGAGTT GATATAAAAT ATAGAACTAC TATAATATTA 2100
GCAACTTGGA GCAGCAAGTT CTTGACTTGG GAAAGTAGGA ATTCCTCTCA TTAAGAGATG 2160
TTTGCCCACA GGGAATGCTG CATAGAAAAG AATTTGGCTG GAACTCTTTT TTTCCACTAT 2220
GACTCCATTC ACACTTGAAT TGTTTCCTTT TACTTTTCTT TTTCTTTCTT TCTTTTTTTT 2280
TTTTTTTTTT GAGACAGAGT CTCGCTCTGT CACCCAGGCT GGAGTGCAGT GGCATGATCT 2340
CAGCTCACTG CAACCTCCGC CTCTCAGGTT TAAGCGATTC TCCTGCCTCA GCCTCCAGAG 2400
TAGCTGGGAT TACAGGCGCG CACCACCATG CCCGGCTAAT TTTCACATTT TTAATAGAGA 2460
TGGGGTTTTG CCATGTTGGC CAGGCTGGTT TTGAACTGCT GACTTCAACT GATCCACCTG 2520
TCTGGGTCTC CCAAAGTGCT GGGATTACAG GCGTGAACAC AGCATGTTTC CGTTTTCAAA 2580
ATAAGATATG TCCTAATTGC TGTGAATTTT TAAAAGAGAA TTATTTTCCA TGACACATTC 2640
TGTTTTCAGA TGTACTGACT TTAGGAGTTG GTAAATAGTC CTCTAGCAAT GCAAATGCAA 2700