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

TagContent
EnhancerAtlas ID
HS146-00061 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr1:9409310-9411150 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MYCMA0147.3chr1:9409369-9409381CGCCACGTGCTC+6.62
Number of super-enhancer constituents: 13             
IDCoordinateTissue/cell
SE_01570chr1:9408913-9413840Aorta
SE_04130chr1:9409356-9409976Brain_Anterior_Caudate
SE_04130chr1:9410879-9412828Brain_Anterior_Caudate
SE_05237chr1:9410188-9411179Brain_Cingulate_Gyrus
SE_05868chr1:9410111-9413845Brain_Hippocampus_Middle
SE_23818chr1:9409874-9410863Colon_Crypt_2
SE_24876chr1:9410381-9410979Colon_Crypt_3
SE_26667chr1:9409237-9411172Esophagus
SE_32227chr1:9409098-9409825Gastric
SE_32227chr1:9410469-9411187Gastric
SE_37396chr1:9408667-9412943HSMMtube
SE_50208chr1:9408996-9412026Sigmoid_Colon
SE_52461chr1:9409040-9411122Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194104709410770
Number: 1             
IDChromosomeStartEnd
GH01I009349chr194090739411184
Enhancer Sequence
TTTTTCGCTC CTCTCTGCTT CCCCGAGCCC AGCCCTCCCG TGCATGAGAC AGACGCTCCC 60
GCCACGTGCT CGACTTTGAT ATTGGTGACG TGTCCTCTCC CTTTATCCCC CACCTGCTTG 120
TGGCACGATG GGGCCAGAGC TGTGCCGGGC CAGGAGTGGG GGTAGGTGAG TGTGGGGTCA 180
GGGGGCTGTC CCAGCTGAGC TCAACCAGAG AGGCCAAGGG ACGTGGAGCG TGAGAGGCTG 240
AGGCCTTGGC GCCAGCGCCG TAGATGCGTG TCAGATTTGA CAGCTGATCT CTGACACAAG 300
GCGTGCAGGA GCGTGGGTGG GTGGACGGCT TGCCTGCCTT CCTCAGGAGG AAGCTATCCA 360
CGGGACATGT CCTGAGCGAG TGTCAGGGAA CTCGTGCCAC ACACAATCCG CCACCAGCAT 420
CGACTCTTCG ATCCAGATGA GATGCAGCTG TCTTCCGTGA CTCACGGCCT CTGGGCCAGT 480
TGTGTGAGGA AGGTCCTTTC GGGAGTTCCC AACCCACCGT TTTATGGCTG TTTTTCTCTC 540
TTGACCCTTC CTGATCTTTA CTTTAATCTG ATCTTACTTG TGGGAAAATG TTGCTAGGAG 600
TTCCCAACCC AGAGTGACTG GTGAGCTCCC TGTCACCCAT GAGGAGGACG GTCCTGCAGT 660
TAGAGCTCCT GTACATACAT ATGCATACAC ACACACAGAC ACACGCCACA CACGCAGACA 720
CAGGCAGACA CGACACACGT GTACCTACAT GCACACACAG CACATATATA CACACATGAA 780
GACACACCAC ACACATATAC ACACATCCAG ACACACCACA CACACAGATA CATACACGCC 840
TCACATATCT ACACACACAC ACACACCCCT ACCACCCGCA CAGGTACACA CACACATTCT 900
TTCTCCTGGT TGAAATACCC TCACGGCATT TATGCCTGTG ATGAGATTAC AACCTGGTCT 960
TCAGGAAGCA CCAGACATTG GACCCCTGCG TGTGACAGCT GAGCCTTGCA GCCTGAGGGC 1020
TGCGGACAGG AGAACTGTCA TTATTTAGAG TGAGTAGAGT TTGGTGGGGC AGGAGGGGTA 1080
CAGGCCAGGC ATTGGTTTGT TGTGGGGCTT GGCTGAGACA GCTGTGCAGA GGAGGAGGCA 1140
GGCGCGGTCC TGGGGACGTG GTGACTAATG CAAGAGTGTG CTTTTGGGGA TGAAAACTTT 1200
CACTAAGGGA ATGGAGAGCA GGCGCCGCCG GCCAGGGCAC TGCCTGGACT ATGACGCCTC 1260
TGTCCTGCTT GTTAGTCTCA GCTGCTGCCT TTGCTCTCAC TGTGTAGGCA CACAGTGTAC 1320
ACGTGTGTGC ATGTGTGTGC ATGTAGGCAT GCGTGCATGC GTGTGTGTGG TGGGTGGCGG 1380
TGGCAGCAGC AGGGCCACAT CTGTCCTCTG CTCTCCCGTT CCAGCCCTGC AGGGCAGTAC 1440
GAGCCACGCC CTTTGCGTCT GCTCCTCCTG GGTGGGGATG AAGGCTGAGT CCTCCCACCT 1500
CCTGGAAACT CACCAACTGC TCAGCAGTCC CAGGCCCTGA TGCTTCTGTG GCACTGCTGG 1560
GCCCCACAAG GCTTAGGCAT CTGCATTTGC TTCTCAGAGC AGCAGTAAGT GGGGGTGGTC 1620
CCAGAGCTGT GCTGTTCTCC CAGCTCCTGC CTGAAGTGTA GTGCCCGGTG CTGGATGCCC 1680
TCCTGGCCCA GGGATGTCTG TCTTGGTCCA GTGTTAACAG GAGCCATCCA GGCACCTGTG 1740
AATGTTACTT GGTACCTGTG GGTGGTACAC ACCCCCTGTC CTGAGCGCCA TGTCCAGGAA 1800
TTGTGATGAT GGTATTAGCA GTTTTGCATG GGGTCGGCAA 1840