EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS006-03155 
Organism
Homo sapiens 
Tissue/cell
Astrocyte 
Coordinate
chr1:202003060-202005290 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CREB1MA0018.3chr1:202004082-202004094GGTGACGTCAGC+6.14
CREB1MA0018.3chr1:202004082-202004094GGTGACGTCAGC-6.14
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
CGAATAAATG AATGCATCTA CCTGATACCT CATCAAGAAA TTGATGACCA CTAATTATCA 60
TCTTTGAACC TCTGATTGGT GACCTCTGGC AAGGCTGAGG ACCTTTAGCT CTAATCAATG 120
GGCAAAAGGT TGACCTCTTT GCTACTGATT GGCTTTTCCT TTTCATTATA CCCTTGGGCT 180
GGATGGGGAA GCTGTGTGAA TCAACGCTTC ATAAGCCTTC CTCTCTGAGA ACTAGGGCTT 240
CCAAGGAATT GGATATGAAA AGGCAGAGAG GAAGGAGGAG GATATGAGAT GCCAGACGGG 300
GGAGGGTGGG GGGGACAGGT CCCAGAAGAG GTCAGCTGGG ACCCAGGCAG GATGGCATTG 360
TGGCTGCGGG TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC CTTGACTGCT 420
GGGTAATCCG TGGTAAGTAC CCACTGCTCC TGCCTCAGCT TCCCCACCTC TCACATGTGG 480
TTGATCCTCA CAGCCATCTC TTGGGGTTGT TCTGAAGATG AAATGAGATC ATCTATGTAA 540
GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC GTATGGTCTG TCCTTATTTG 600
GGGAATGGGG GTGGAAGGCG CCCAGCAGGG CATGGGGCGT GGTATGGCAG AGCCAGGACT 660
AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG ATTTCCCATG TTCTCACCAT 720
CTACAGAGTC ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC TCACACTAGG 780
TGGAGGAGCC CTCACAGATC TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA GCACCAGGGC 840
CCTGGGACCA GCTGGTGGTT TCCACCAGAG CAGCCTCGGG GTGAATTTAG TCAGGAATGT 900
GCCCTCAGCT CAAGAGAACC CTCCCCAACC TTCCACTCCC CATACCCACC CCCGACCGCA 960
GGTTCCCCAC CCACCCGTGG CCTGGCCAGC AGCAACCTCC ACTAGCTCGC TAGCTCAGTG 1020
ACGGTGACGT CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT TCACCTCTCC 1080
CTGGGGAGAC TGGATTACCT CACCCTGGGA GCAGAGTGAA TGATTAACCA GCTTCATCCT 1140
GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT AGGCCTACAG GGCAAGGGGC TGCATGGTCA 1200
CATACCCTAG TATGCGGGTT CACATACCCC AGCCGGGGCT GGGGTATGTG ACCGCCCCGT 1260
CCTTGGCCAC TGCCCTCTTA TCTGCATCAC TGCTCACAAG TGTCATAAAA ATTTGTCTAC 1320
AGCATATATA AATATACATA TGACGTGGAA GGCTTCCGAT GGCAAATAAC ATTTTCCATT 1380
TTGCCTAAGC TTGGGTGGCT TTTTATTCAT CTATTGTTGT TTTAAGTACA CATTTCCATC 1440
TAAACTTAGA TGTATGTTTA GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT CCCAGTACCT 1500
TTTAGGGGGT TGAGGCGGGT GGATCATTTG AGGCCAGCAG TTCAAGACCA GCCTGGCCAA 1560
CATGATGAAA CCTCGTCTCT ACTAAAAAAT ACAAAAATTA GCTGGGTGTG GTGGCAGGCG 1620
TCTGTAATCT CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGAGGCGG 1680
AGGCTGCAGT GAGCTGAGAT TGCACCATTG CACTCCAGCC TGGGCAACAG AGTGACATTC 1740
TGTCTCAAAA ACAAAAACAA AAACAAAACA AAAAAAATAA ACTTAGATGT ATATTTAAAA 1800
ATTGCTTTTT ACCCCTGAAG GTCTCAGCAT CCTACCTGCT CTATTCATTA GTGTTTAGAT 1860
TACCCATGAC ACCAGAAGGA CTTCCCAACC CAGAAAAAGA TCCAGGAGTT GATATAAAAT 1920
ATAGAACTAC TATAATATTA GCAACTTGGA GCAGCAAGTT CTTGACTTGG GAAAGTAGGA 1980
ATTCCTCTCA TTAAGAGATG TTTGCCCACA GGGAATGCTG CATAGAAAAG AATTTGGCTG 2040
GAACTCTTTT TTTCCACTAT GACTCCATTC ACACTTGAAT TGTTTCCTTT TACTTTTCTT 2100
TTTCTTTCTT TCTTTTTTTT TTTTTTTTTT GAGACAGAGT CTCGCTCTGT CACCCAGGCT 2160
GGAGTGCAGT GGCATGATCT CAGCTCACTG CAACCTCCGC CTCTCAGGTT TAAGCGATTC 2220
TCCTGCCTCA 2230