EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS120-00009 
Organism
Homo sapiens 
Tissue/cell
LNCaP-abl 
Coordinate
chr1:1002500-1005080 
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr1:1004737-1004751GTGGGGGCGTGGCC-6.39
KLF16MA0741.1chr1:1004739-1004750GGGGGCGTGGC-6.62
KLF5MA0599.1chr1:1004502-1004512GCCCCGCCCC+6.02
KLF5MA0599.1chr1:1004521-1004531GCCCCGCCCC+6.02
KLF5MA0599.1chr1:1004157-1004167GGGGCGGGGC-6.02
KLF5MA0599.1chr1:1004196-1004206GGGGCGGGGC-6.02
NRF1MA0506.1chr1:1004721-1004732GCGCCTGCGCG+6.14
Pou2f3MA0627.1chr1:1002525-1002541TATCATTTGCATAGCA-6.09
RFX1MA0509.2chr1:1004774-1004790CGTCGCCATGGTGACC+6.11
RFX1MA0509.2chr1:1004774-1004790CGTCGCCATGGTGACC-6.12
RFX2MA0600.2chr1:1004774-1004790CGTCGCCATGGTGACC+6.2
RFX2MA0600.2chr1:1004774-1004790CGTCGCCATGGTGACC-6.2
SP1MA0079.4chr1:1004499-1004514CAAGCCCCGCCCCTC+6.34
SP2MA0516.2chr1:1004498-1004515GCAAGCCCCGCCCCTCA+6.23
SP3MA0746.2chr1:1004738-1004751TGGGGGCGTGGCC-6.57
SP4MA0685.1chr1:1004499-1004516CAAGCCCCGCCCCTCAT+6.24
SP8MA0747.1chr1:1004738-1004750TGGGGGCGTGGC-6.11
ZNF263MA0528.1chr1:1003831-1003852CCTTCCTCCTCCTCCTGCTCG-6.88
ZNF263MA0528.1chr1:1003819-1003840CCCTCCCCATTTCCTTCCTCC-6.89
ZNF263MA0528.1chr1:1003825-1003846CCATTTCCTTCCTCCTCCTCC-7.03
ZNF263MA0528.1chr1:1003822-1003843TCCCCATTTCCTTCCTCCTCC-8.3
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_24070chr1:1002554-1005867Colon_Crypt_2
SE_24817chr1:1002490-1006081Colon_Crypt_3
SE_27529chr1:1001798-1011077Esophagus
SE_34539chr1:1002321-1004360HCT-116
SE_34539chr1:1004454-1006480HCT-116
SE_41944chr1:1001963-1005965LNCaP
SE_58139chr1:1003761-1004209VACO_9m
SE_58139chr1:1004236-1004768VACO_9m
SE_58139chr1:1004812-1005267VACO_9m
SE_65935chr1:1001682-1006445Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr110034591003600
Number: 1             
IDChromosomeStartEnd
GH01I001066chr110018371006486
Enhancer Sequence
GCATAATATT TGTGTGTCGT TTGCATATCA TTTGCATAGC ATTTGCATGG ACTTGTTTGT 60
CCTCTGTTAA CAGCAGCAGT TGGCCTCATT CCCTTTCAGA CTGACCCTGA GGAGGAGCCG 120
GGCCATGGCA GGGGCAGGGT GGACATCCCT TGTGGCCCTG CCCCGCCGCA CCTGCACCTG 180
CACAGCCCGC GTGGGCCCGC CCCGCCGCAG CTGAAGTGCA CCACCATGGG CCCGGCCCGC 240
GGCTCGCGGC TCGCGGCTCT GGGCCCGGTT CACCTCGTCC CGGAAGCCGA GGACGCCGGC 300
GGGATCGGTC CGGACGCCGT AGTCCGGCCA GCCGAAGTAC TGGAAGTGCT GCACCGTACG 360
CTGTGGCTCC TCCCCGCGGG GCAGGGCCTC GCGGGCGCAG GGTGTACATC GCCTGCAGGG 420
CTGTCTGCAG GCCTGTCTGC AGGCCACGGT GGCTGCTTTC TGGGCCACGG TGCACCAGGA 480
GAACACGCGT GTCATCGTCA TGACCACCAG GGAGATGGAG CGGGGCCGGG TAGGGGTGCG 540
GTGCCAGTGC TCCCAGTGCC CATCCCACCC CGTGCATCTT CGGCTGCCCA AGGCCCTTCC 600
CGACCAGGCC AAGGAGGCTG TGGGACGCCG TGGGAGTGGG GAGGCTCCCA CAGAGCCCCG 660
TGGCTGCACG TACACACCTG CGTCTCTGCA GGTCGCAGGG GCGGGGTGCC GAGGTGCTGC 720
CAGCAAGGCT GATGCAAAGC GCTCCCCTCG GAACAAGTGT TTCCGGGACT GGCCAGAGCT 780
GCCCGGCAGC CAAGAGTTCG GCCGTGTGCA CATGCGCGTC CTCGGCAAGG GCCAGGCCCA 840
GGGCTACTGC GTGCGGGAGC TGCAGGTGTG GCGGCCGGGC CAGGTGAGCC TGGCGGCTGT 900
GGAGCGTGCC TGCTGTCGGC CTGCACTGGG AGACCCCACA CCTGCCTGCA TCCAACCCCA 960
CTGCCTTTGG GGGCTTCCAC ACCCCTCAAC CCAGGAGGTG CATTCCAAGC CTGGACAGGG 1020
GTCACTGACG TGGCCACATT CTCAGCCCTG GGCTGGCGGC CGCTCCTCCC ACACACCTCT 1080
CCAACTGCAG CTTTGGTCTC CGTTGTATAC CAGAGACGCC CATTTCTGCT CCGGGCAGAT 1140
TACCTCGTGT TCCCTCCAGC CCCCGCCCAG TGTGTGTGGG GGGGTCCTCC AGGACCCCAT 1200
GGACCCCTCA CATTTGGTTT TTCCTTATAA AATAACTGTC CTCACAGCCT GCTTCGCCCG 1260
CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA CCTGAGCCAC CTGGGGCCAT CTCGGCGCCC 1320
CCTCCCCATT TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG 1380
GCACTCCCGG AAACCCAGCT GTGCCTCAGC CTCCTCCTCC CACCCTGGGG TCACACTCAC 1440
CGCTTGCCCC GCTCAGGAGG AGCCACAGCG TACGGTGCAG CACTTCCAGT ACTTCGGCTG 1500
GCCGGACTAC GGCGTCCGGG CCGATCCCGC CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA 1560
CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG GCCCATGGTG GTGCACTTCA GCTGCGGCGG 1620
GGCGGGCCCA CGCGGGCTGT GCAGATGCAG GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG 1680
CAGGTGCAGG TGCGGCGGGG CGGGGCCACG CGGGACGACG AGGGCGGAGC CATCGGGTGG 1740
GCGGGGGCGC CCCCGCCCCC GCCCCCCACT CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG 1800
TGGGGGCATC GGATGCACGG GCACCATCAT CGTGATTGAC ATCCTGGTGG ACGTCATCCG 1860
CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT GCCCTGCTAT AGCCCCACCC 1920
CTCCGGGCGA CCCCACCCCT CCGGACGACC CCACCCCTCA GGACGACCCC ACCCCTCAGG 1980
ACGACCCCAC CGCTACCGGC AAGCCCCGCC CCTCATCAGC AGCCCCGCCC CTGCCTGCCG 2040
GCACCTTCCC CCCATCCGTA GCCCCTCCCC AAGCGCGCTT GTCCGCAGGG CTGGACTGCG 2100
ACACCGACGT CCCGAAGACG ATCCAGCTGG TTTGGCGGCA GCACTGGGGA ATGGTGCAGA 2160
CGGAGGCTCC GTACAAGTTC ACGTACCTGG CGCTGCAGCG GCACATCCGG GGCGAGTAAC 2220
TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC 2280
CATGGTGACC GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT CAGGAGCGCG AGAACCAAAA 2340
CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG 2400
TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG GACTGGGACG TGCGGGGTGC 2460
AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC TGGGACGGCG AGGACGCGAA 2520
CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC CCGGCCTAGC CGCGCCCGCG 2580