EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-05294 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr1:202003010-202005510 
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
GCTTTGCTCA CAATGTGTAT CCCACTGAAG ACATCCAATA AACAATTTAT CGAATAAATG 60
AATGCATCTA CCTGATACCT CATCAAGAAA TTGATGACCA CTAATTATCA TCTTTGAACC 120
TCTGATTGGT GACCTCTGGC AAGGCTGAGG ACCTTTAGCT CTAATCAATG GGCAAAAGGT 180
TGACCTCTTT GCTACTGATT GGCTTTTCCT TTTCATTATA CCCTTGGGCT GGATGGGGAA 240
GCTGTGTGAA TCAACGCTTC ATAAGCCTTC CTCTCTGAGA ACTAGGGCTT CCAAGGAATT 300
GGATATGAAA AGGCAGAGAG GAAGGAGGAG GATATGAGAT GCCAGACGGG GGAGGGTGGG 360
GGGGACAGGT CCCAGAAGAG GTCAGCTGGG ACCCAGGCAG GATGGCATTG TGGCTGCGGG 420
TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC CTTGACTGCT GGGTAATCCG 480
TGGTAAGTAC CCACTGCTCC TGCCTCAGCT TCCCCACCTC TCACATGTGG TTGATCCTCA 540
CAGCCATCTC TTGGGGTTGT TCTGAAGATG AAATGAGATC ATCTATGTAA GAAGCTGGCA 600
CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC GTATGGTCTG TCCTTATTTG GGGAATGGGG 660
GTGGAAGGCG CCCAGCAGGG CATGGGGCGT GGTATGGCAG AGCCAGGACT AAGGGTCTGT 720
AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG ATTTCCCATG TTCTCACCAT CTACAGAGTC 780
ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC TCACACTAGG TGGAGGAGCC 840
CTCACAGATC TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA GCACCAGGGC CCTGGGACCA 900
GCTGGTGGTT TCCACCAGAG CAGCCTCGGG GTGAATTTAG TCAGGAATGT GCCCTCAGCT 960
CAAGAGAACC CTCCCCAACC TTCCACTCCC CATACCCACC CCCGACCGCA GGTTCCCCAC 1020
CCACCCGTGG CCTGGCCAGC AGCAACCTCC ACTAGCTCGC TAGCTCAGTG ACGGTGACGT 1080
CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT TCACCTCTCC CTGGGGAGAC 1140
TGGATTACCT CACCCTGGGA GCAGAGTGAA TGATTAACCA GCTTCATCCT GGAGGGCCTC 1200
AAAGGCCCGT CCTGGGGTGT AGGCCTACAG GGCAAGGGGC TGCATGGTCA CATACCCTAG 1260
TATGCGGGTT CACATACCCC AGCCGGGGCT GGGGTATGTG ACCGCCCCGT CCTTGGCCAC 1320
TGCCCTCTTA TCTGCATCAC TGCTCACAAG TGTCATAAAA ATTTGTCTAC AGCATATATA 1380
AATATACATA TGACGTGGAA GGCTTCCGAT GGCAAATAAC ATTTTCCATT TTGCCTAAGC 1440
TTGGGTGGCT TTTTATTCAT CTATTGTTGT TTTAAGTACA CATTTCCATC TAAACTTAGA 1500
TGTATGTTTA GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT CCCAGTACCT TTTAGGGGGT 1560
TGAGGCGGGT GGATCATTTG AGGCCAGCAG TTCAAGACCA GCCTGGCCAA CATGATGAAA 1620
CCTCGTCTCT ACTAAAAAAT ACAAAAATTA GCTGGGTGTG GTGGCAGGCG TCTGTAATCT 1680
CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGAGGCGG AGGCTGCAGT 1740
GAGCTGAGAT TGCACCATTG CACTCCAGCC TGGGCAACAG AGTGACATTC TGTCTCAAAA 1800
ACAAAAACAA AAACAAAACA AAAAAAATAA ACTTAGATGT ATATTTAAAA ATTGCTTTTT 1860
ACCCCTGAAG GTCTCAGCAT CCTACCTGCT CTATTCATTA GTGTTTAGAT TACCCATGAC 1920
ACCAGAAGGA CTTCCCAACC CAGAAAAAGA TCCAGGAGTT GATATAAAAT ATAGAACTAC 1980
TATAATATTA GCAACTTGGA GCAGCAAGTT CTTGACTTGG GAAAGTAGGA ATTCCTCTCA 2040
TTAAGAGATG TTTGCCCACA GGGAATGCTG CATAGAAAAG AATTTGGCTG GAACTCTTTT 2100
TTTCCACTAT GACTCCATTC ACACTTGAAT TGTTTCCTTT TACTTTTCTT TTTCTTTCTT 2160
TCTTTTTTTT TTTTTTTTTT GAGACAGAGT CTCGCTCTGT CACCCAGGCT GGAGTGCAGT 2220
GGCATGATCT CAGCTCACTG CAACCTCCGC CTCTCAGGTT TAAGCGATTC TCCTGCCTCA 2280
GCCTCCAGAG TAGCTGGGAT TACAGGCGCG CACCACCATG CCCGGCTAAT TTTCACATTT 2340
TTAATAGAGA TGGGGTTTTG CCATGTTGGC CAGGCTGGTT TTGAACTGCT GACTTCAACT 2400
GATCCACCTG TCTGGGTCTC CCAAAGTGCT GGGATTACAG GCGTGAACAC AGCATGTTTC 2460
CGTTTTCAAA ATAAGATATG TCCTAATTGC TGTGAATTTT 2500