EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-27072 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr19:10137580-10138830 
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr19:10138559-10138578TTGCGCCCTCTGGTGTCCA-6.9
EWSR1-FLI1MA0149.1chr19:10137724-10137742TTTTTTTTCCTTCCTTCC-6.18
EWSR1-FLI1MA0149.1chr19:10137756-10137774CCTCCCTCCCTTCCTCCC-6.92
EWSR1-FLI1MA0149.1chr19:10137752-10137770CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr19:10137748-10137766CCTTCCTCCCTCCCTCCC-7.28
EWSR1-FLI1MA0149.1chr19:10137728-10137746TTTTCCTTCCTTCCTTCT-7.52
EWSR1-FLI1MA0149.1chr19:10137744-10137762CTTTCCTTCCTCCCTCCC-7.57
EWSR1-FLI1MA0149.1chr19:10137768-10137786CCTCCCTTCCTTCCTTCT-7.79
EWSR1-FLI1MA0149.1chr19:10137740-10137758CCTTCTTTCCTTCCTCCC-7.85
EWSR1-FLI1MA0149.1chr19:10137760-10137778CCTCCCTTCCTCCCTTCC-8.06
EWSR1-FLI1MA0149.1chr19:10137736-10137754CCTTCCTTCTTTCCTTCC-9.17
EWSR1-FLI1MA0149.1chr19:10137732-10137750CCTTCCTTCCTTCTTTCC-9.47
EWSR1-FLI1MA0149.1chr19:10137764-10137782CCTTCCTCCCTTCCTTCC-9.83
Foxd3MA0041.1chr19:10137802-10137814AAACAAATAATC-6.07
ZNF263MA0528.1chr19:10137747-10137768TCCTTCCTCCCTCCCTCCCTT-6.46
ZNF263MA0528.1chr19:10137743-10137764TCTTTCCTTCCTCCCTCCCTC-6.58
ZNF263MA0528.1chr19:10137751-10137772TCCTCCCTCCCTCCCTTCCTC-6.63
ZNF263MA0528.1chr19:10137767-10137788TCCTCCCTTCCTTCCTTCTCT-6.79
ZNF263MA0528.1chr19:10137760-10137781CCTCCCTTCCTCCCTTCCTTC-6.93
ZNF263MA0528.1chr19:10137755-10137776CCCTCCCTCCCTTCCTCCCTT-7.27
ZNF263MA0528.1chr19:10137739-10137760TCCTTCTTTCCTTCCTCCCTC-7.37
ZNF263MA0528.1chr19:10137764-10137785CCTTCCTCCCTTCCTTCCTTC-7.39
ZNF263MA0528.1chr19:10137736-10137757CCTTCCTTCTTTCCTTCCTCC-7.41
ZNF263MA0528.1chr19:10137752-10137773CCTCCCTCCCTCCCTTCCTCC-7.9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191013848810138727
Number: 1             
IDChromosomeStartEnd
GH19I010027chr191013782910138918
Enhancer Sequence
CACAAGGTTC CCTTCCTCAT TTCCTTCATG CGCTCAAATA CCACCTCCTC CAAGAGGTCC 60
TCCAGGCTCA CCTCAAGATA GCACACTGTC CCTTTATTTT CTTACGTGTT TTATTTCCCA 120
TGATCTGACA TGGTTCTCTC TCTTTTTTTT TTCCTTCCTT CCTTCTTTCC TTCCTCCCTC 180
CCTCCCTTCC TCCCTTCCTT CCTTCTCTTT CTTTCATTCT AAAAACAAAT AATCATAGAA 240
ACGGGGGTCT TGCTTTATTG AGCAGGCTGC TTTTGAATTC CTGGGCTCAA GTGATCCTCC 300
CACCTCGGCC TCTCAAAGTG CTGGGATTAC AGACATGAGC CACCACGCCC GGCAGGCATA 360
TACCACTGTT TCTTGCTTGT CTCCACCCAC TAAAATGTCA GCTCCATGGG CAGGGGACTG 420
TTGTCTATTT GCTCTACCCA CATCACCAGC ACCGTGGAAA CCAAAAAATG ACTCAAGGAG 480
TTAACCAAGC TGGCACATCC TGGCAGTACA GTCCACCCTG AGAAGCTCCT GACACCTCCT 540
ACCTGGACAA GACAGGGTAC TTCTCTGACC CTCAGTTTCT TCATCTGTGA AATGGAACTT 600
GCCAGGGAGA AAGTTATATT AAGGGCTGGA ATGTAGTCGG GGTCTAATAA ATTAGAGCCC 660
TTAATAGTTA TGTTGATGGT AGCCTTATTC CTTGGTCTCC TGGGTCCTGC CCGGCCTTCC 720
CTGGGAAGCT CTGAGCTCAA AGCCCTGGAG GAGGGAGTAA AACCAGAGGC TGCATCTCTG 780
CAAGGACACA TCCCTGCAAG TCCACCCCTC CCGCCCGCGC CTTCTCGGTG CAAACTCCCG 840
ATCCCAGGGA GGGGAAGGCG GGCGGAATCT GAGCGGCAGG CGCAGCTGCT CCGGGCGGGC 900
GGCCAAGGTT CCCTCCCTCG AGCACTGGCA TTCCTGAGGG AGGGGCCGAG CGCAGCTGCC 960
CGCCTGGCCG GAGGCTCGCT TGCGCCCTCT GGTGTCCAAG TACGAGAGGC CACGTGGACT 1020
TGCGCACCAG CAGCCGGTCT GTTCTAGGCC ACTGTCTGCA GCTCAGGTGG ACCTGGGTGG 1080
AGCTAGGTCT ACCCCCTACC TTTCTTGGGC TCCCTTTTCT TATCCGGGTT CACGAACTCA 1140
GCTTCCATCA CTAAACTTGC TGTGTGACCC TGAGCAAGAC ACTCAACCTC CCTGTACCAC 1200
AGTTTCTTAG CTGTGCAATT TGGGACAGGA TCCTTTACCT TTTTAGTGCC 1250