EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-15341 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr15:69915610-69917990 
Target genes
Number: 6             
NameEnsembl ID
TF binding sites/motifs
Number: 29             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr15:69916976-69916994CCCTCCTTCTCTCCCTCC-6.03
EWSR1-FLI1MA0149.1chr15:69916985-69917003TCTCCCTCCCTCCCTTCC-6.25
EWSR1-FLI1MA0149.1chr15:69917005-69917023CCTGCCTGCCTTCCCACC-6.26
EWSR1-FLI1MA0149.1chr15:69917009-69917027CCTGCCTTCCCACCTTTC-6.29
EWSR1-FLI1MA0149.1chr15:69916993-69917011CCTCCCTTCCTGCCTGCC-6.53
EWSR1-FLI1MA0149.1chr15:69916953-69916971CCTCCCTTCCTGCCTTTC-6.69
EWSR1-FLI1MA0149.1chr15:69916989-69917007CCTCCCTCCCTTCCTGCC-6.72
EWSR1-FLI1MA0149.1chr15:69916937-69916955CCCTCCTTCCTGACTTCC-6.88
EWSR1-FLI1MA0149.1chr15:69916997-69917015CCTTCCTGCCTGCCTGCC-6.92
EWSR1-FLI1MA0149.1chr15:69916961-69916979CCTGCCTTTCTTCCTCCC-6.95
EWSR1-FLI1MA0149.1chr15:69916941-69916959CCTTCCTGACTTCCTCCC-7.11
EWSR1-FLI1MA0149.1chr15:69916945-69916963CCTGACTTCCTCCCTTCC-7.14
EWSR1-FLI1MA0149.1chr15:69916949-69916967ACTTCCTCCCTTCCTGCC-7.1
EWSR1-FLI1MA0149.1chr15:69917001-69917019CCTGCCTGCCTGCCTTCC-7.45
EWSR1-FLI1MA0149.1chr15:69916929-69916947CCTTCCCTCCCTCCTTCC-8.15
EWSR1-FLI1MA0149.1chr15:69916925-69916943CCTTCCTTCCCTCCCTCC-8.45
EWSR1-FLI1MA0149.1chr15:69916957-69916975CCTTCCTGCCTTTCTTCC-8.89
EWSR1-FLI1MA0149.1chr15:69916921-69916939CCTTCCTTCCTTCCCTCC-9.47
EWSR1-FLI1MA0149.1chr15:69916917-69916935ACTTCCTTCCTTCCTTCC-9.88
FOSL1MA0477.1chr15:69916363-69916374AGTGACTCATG+6.14
Sox6MA0515.1chr15:69917494-69917504AAAACAATGG-6.02
ZNF263MA0528.1chr15:69916964-69916985GCCTTTCTTCCTCCCTCCTTC-6.05
ZNF263MA0528.1chr15:69916980-69917001CCTTCTCTCCCTCCCTCCCTT-6.28
ZNF263MA0528.1chr15:69916972-69916993TCCTCCCTCCTTCTCTCCCTC-6.32
ZNF263MA0528.1chr15:69916957-69916978CCTTCCTGCCTTTCTTCCTCC-7.12
ZNF263MA0528.1chr15:69916921-69916942CCTTCCTTCCTTCCCTCCCTC-7.27
ZNF263MA0528.1chr15:69916976-69916997CCCTCCTTCTCTCCCTCCCTC-8.3
ZNF263MA0528.1chr15:69916925-69916946CCTTCCTTCCCTCCCTCCTTC-8.92
Znf423MA0116.1chr15:69916586-69916601GCACCCCTGGGTGGG-6.03
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr156991640069917075
Number: 1             
IDChromosomeStartEnd
GH15I069624chr156991636469916890
Enhancer Sequence
ATTTGGTGCA TTGCTTGCAG AAGACTTTAG ATCCTGGAGA TTTTAGAACC ACCATGCTCT 60
TAGGTGTAGA AGGAAAAGGC TGGTTCCTGT TTGGGGGACA CTAGAAACAG AAAGAAATAA 120
TGGAACACTG CCTGGCTTTG ACTGTAAGCT GCCTTAAGTT GGAATCTAGT GTGCCTTTGG 180
TTAAGTTATT TATACTCTTG GAATTTCAGC TTCTTTACCT GAGAGAGACA ACGTCCTACT 240
TCTCCTGGGG ATGGTCTTGA AGACTGAATG GCTCTATAAA ACTTGGCCCA GTGCCTGGAG 300
CACAGATGCT CTCAGCAAAC ATACTCTTGT CCCCACCCCA GAAAGCTTCC AGGTCATTCT 360
GATCTCTCTG GTGAAAGGGA AGGATCTCTT ATTGTCTGAA CCACACATAT TTAAAGAAAC 420
TAAAACTGTG TGTCCAGGGA ATTATGCTGA TTATGTTAAT TTCTACCTTG ATTGGTATAT 480
AGCACATAGA TTAACTAGAA CTGCAGAGGG ATGGGGAGAT GCTAAAGTCA CCTCCTAGCC 540
TCCCCCAGCA CTGGGCTCTG GGCTCCCTAC CTCCTGCCTG ACATGGGTGG CCCTAGTGCC 600
CATTGGGTCT GCTAACCAGG TCCTGGCTGA AGATATGAGG GAGGCCTAGG GGACTCTTGG 660
GCTGGGACTG AGATGGTTTA AAGAAAAAAC ATGTGAGAAC CTGTGTAATA TTGGGATGTG 720
GGAGAGGTGA TAGGGCTGAG AGGCACCGAA GGCAGTGACT CATGGTAGTT CTGCAGCTTG 780
AGGTTATTAG GTGGCATCAA TCTGAAAAGA AACTGGGGCT CACCACCCTT TCCCAGCCAC 840
TCCCTACGTC AATTTCTCAG CAGGTTGTTG TCCATTTCCA TGGGGAGACA TTTCTGTTGT 900
TTCCTCTGGT GAATTCCAGC ATGAGCTAGT CTCTCCTTGG GTTGTTATTT GGGGCTTGGT 960
GAAGGGGGGA TTCTGAGCAC CCCTGGGTGG GAGTCACCAT GTTGTCTGAA GACACCATGT 1020
GACTAAGTGT TAGACTCAGT GAACTCATGT CCAAGAAGGT TGGGGTGTGG TGTGGAAATT 1080
ACTAATTTTA GAGTCAGATT CCCCTGGGTT CCAGCCTTAG CTCAGTCACG TGGAAGCTGT 1140
GCCTCACTGG GCAGTTACTT CACCTCTGTG ATGTTTTTTG GAACACCAGC TTTGTATTGG 1200
GGTTTTCACA GGAGTTATGT CTTCTAATTC TCACAACCAG CCCGATGTAA GGGATGTTAT 1260
TCCTATCTCA CAGATGATGA AAAACTGAGC CTTCAAGAAG TGAAGTAACT TCCTTCCTTC 1320
CTTCCCTCCC TCCTTCCTGA CTTCCTCCCT TCCTGCCTTT CTTCCTCCCT CCTTCTCTCC 1380
CTCCCTCCCT TCCTGCCTGC CTGCCTTCCC ACCTTTCTGC CATCTTCCCT CCCTCTCCTC 1440
TCATTCTTGA TCATTCCCAC TCTTTCTTTC AAACATGTTT TAAGTGCCTG CTAGTTTCAC 1500
CTACATGATC ATCTTTTAAT ATATTTTTGA GTTCAAAGAC ACCTACTTGA AGTGCTTTCC 1560
TTCCTCCATC TGGGACATGC TCCTTGGGTC CAGACCAACT CTGTTCTCCC AAGGGAAGAG 1620
AAGCAGCTCT CACAGAGGAG CTCCCTTCTT CCGCAGAATC AGATGCTGCC CTTGTGGCCA 1680
GTTGGGTTCC CACCCACCTG ATTCTGGAGC CCTGGACCAG AGCCCTACGT TCACCATGGG 1740
AAGAGACCTT GTGATAAGCC ACTCCTGAAG GCATGGCCTA ACTCTGGACA CAGGTGGACA 1800
GTGGGTCACC ACCAGGCTTG GCCACCACCC AGATCCCCTT GGACCAGGAG ATCAAGGCTT 1860
CGTGCTCCAT CAAGGACATG AAACAAAACA ATGGGGAGGA ATAAAACAGG AGACCTAAAA 1920
AGCAAGTATT CTTGTCCCTT GTCCAGACTT TGGAAACATT TTGTCTTGAG AAAAATCTGA 1980
TTCACAGAGG GGGCTTGGGG AAGGGGGCTG CAAAGGCAGG TTGAGGAGCT CAGTAAATAC 2040
CAGAGAGTGA GCCTGGTAGG AGACTCTGTT CCTCCAGCTC TGAAATGACT GTGGGAACAT 2100
GAAAACAAGT TTGTTTTTAA CCATCTACCA GCACATGGGA GGAGAGAAAG TTCTGGGATT 2160
TCCCTCTCTC TCCTCTCTTC CTGAATTGAA GAAAACTTGG CCATTTGTCC TGCTCTGGTT 2220
TCCAATACTG TCTCCTGGGT CCTTAGGAGG TGCTAAGCCG AGTGGCCAGC ACACACAGAG 2280
GGTGTTATTC CAGCTTCAGG TCATGCTGAT GGAAACTAGA AACCAAGTCC TACCCAAAGC 2340
AGAATGAAAT ACACACCCCA CATCATCATC ATATGGTTTG 2380