EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS138-11493 
Organism
Homo sapiens 
Tissue/cell
MSC_BM 
Coordinate
chr13:73847240-73849600 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs77792117chr1373847475hg19
TF binding sites/motifs
Number: 34             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr13:73848810-73848828GGAAGGAAGGAAGGAAGA+10.05
EWSR1-FLI1MA0149.1chr13:73848806-73848824GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr13:73848839-73848857GGAGGAAGGGAGGGAAGG+6.03
EWSR1-FLI1MA0149.1chr13:73848822-73848840GGAAGAGAGGGAGGGAGG+6.14
EWSR1-FLI1MA0149.1chr13:73848838-73848856GGGAGGAAGGGAGGGAAG+6.27
EWSR1-FLI1MA0149.1chr13:73848843-73848861GAAGGGAGGGAAGGAGGG+6.33
EWSR1-FLI1MA0149.1chr13:73848818-73848836GGAAGGAAGAGAGGGAGG+6.73
EWSR1-FLI1MA0149.1chr13:73848847-73848865GGAGGGAAGGAGGGAGGG+6.84
EWSR1-FLI1MA0149.1chr13:73848834-73848852GGGAGGGAGGAAGGGAGG+6.88
EWSR1-FLI1MA0149.1chr13:73848794-73848812AAAAGGAAGGGAGGAAGG+7.03
EWSR1-FLI1MA0149.1chr13:73848830-73848848GGGAGGGAGGGAGGAAGG+7.28
EWSR1-FLI1MA0149.1chr13:73848851-73848869GGAAGGAGGGAGGGAAAG+7.5
EWSR1-FLI1MA0149.1chr13:73848814-73848832GGAAGGAAGGAAGAGAGG+7.82
EWSR1-FLI1MA0149.1chr13:73848802-73848820GGGAGGAAGGAAGGAAGG+9.47
EWSR1-FLI1MA0149.1chr13:73848798-73848816GGAAGGGAGGAAGGAAGG+9.6
FOXC1MA0032.2chr13:73847791-73847802TATGTAAATAT+6.62
IRF1MA0050.2chr13:73849036-73849057ATAGAGAAAGTGAAAGAGATT-7.3
TEAD1MA0090.2chr13:73848188-73848198ATGGAATGTG-6.02
ZNF263MA0528.1chr13:73848811-73848832GAAGGAAGGAAGGAAGAGAGG+6.11
ZNF263MA0528.1chr13:73848777-73848798GGAGAAGGAAAAGAGAGAAAA+6.19
ZNF263MA0528.1chr13:73848848-73848869GAGGGAAGGAGGGAGGGAAAG+6.1
ZNF263MA0528.1chr13:73848800-73848821AAGGGAGGAAGGAAGGAAGGA+6.28
ZNF263MA0528.1chr13:73848795-73848816AAAGGAAGGGAGGAAGGAAGG+6.31
ZNF263MA0528.1chr13:73848844-73848865AAGGGAGGGAAGGAGGGAGGG+6.46
ZNF263MA0528.1chr13:73848815-73848836GAAGGAAGGAAGAGAGGGAGG+6.78
ZNF263MA0528.1chr13:73848840-73848861GAGGAAGGGAGGGAAGGAGGG+6.8
ZNF263MA0528.1chr13:73848807-73848828GAAGGAAGGAAGGAAGGAAGA+7.03
ZNF263MA0528.1chr13:73848828-73848849GAGGGAGGGAGGGAGGAAGGG+7.19
ZNF263MA0528.1chr13:73848839-73848860GGAGGAAGGGAGGGAAGGAGG+7.33
ZNF263MA0528.1chr13:73848803-73848824GGAGGAAGGAAGGAAGGAAGG+7.42
ZNF263MA0528.1chr13:73848832-73848853GAGGGAGGGAGGAAGGGAGGG+7.5
ZNF263MA0528.1chr13:73848819-73848840GAAGGAAGAGAGGGAGGGAGG+7.61
ZNF263MA0528.1chr13:73848852-73848873GAAGGAGGGAGGGAAAGAAAA+7.78
ZNF263MA0528.1chr13:73848836-73848857GAGGGAGGAAGGGAGGGAAGG+7.88
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr137384792173848283
chr137384846273848574
Number: 1             
IDChromosomeStartEnd
GH13I073272chr137384639473850306
Enhancer Sequence
CCTTCTCTGC TCCTTCAGAA TAGCAAAAAT AGCTTGTATA TACTAAGGGC TTATCAAGAG 60
CCCCAAAATG TCCTGTACAT TTTTATATGC ATTATCTTGT TTCATCCATA CAGCAGTCCT 120
GTAAAGTAGG CAGAAGGGAA AACTGAGGCT TAGAGAGATG AAGGCACTTG CCCAAGGCCA 180
CCCAGTTAGG AAATAATAGA GCCAAGATGC AAGCCCAGCA ATCTAACTCC AGAATCTAGA 240
GGCTTGACTT TCATTATGAA CACTGTTTTG TGTAGAACTT CTGTGTGAGT TGAGTTCGTG 300
TGAATGCAAA GCAGGTTCTG GTCATGGGAC TAGAAAGGCC TTGATAAATT CTCTTTTACT 360
GCATGACAGG CAGCAGCACC TCAGTGGGAT GACTTCAACA CAAACTGCCC AATGGCAGTG 420
CCATGATGAA ATATGATAGA GAATAATGTA CCATAAAATT TTTAAACTGG AGAGAATCTG 480
TTAGGCCATC TATATTACAT ATATAATACA CATATGTGTA TATGAGACAT GCAGATATAC 540
ATGTATGTGT GTATGTAAAT ATGTATTCAA TAGTATCAGA GATTCTTAAT TCAAGAATAT 600
ACTTGACTAG ATATAAATAG CATTCTTTGA AGGTGACATC TTCCTGATAA GACACTTAAA 660
AGATGTTCTC AATTTTGTAT ATTCGGAATC TTCTGGAGAT TTGTGCATGT ATGTATAAGT 720
GCGTGCACAC TTCCATAAGA CTAATTCTTT TTCTTGCTAC TCGTGGTACC GTCCTTATAA 780
ACCTATGATT CACAACAGGA ATGTAGCTTG GAACTCCTGC TATGTAAGCA GCTGCAGATA 840
CTTCAAATAC CAGTGTACAT GTGATCCAGG AGTTGCTATA AATTTGCCCC TAAAAATAAA 900
GTAACAAGTG ACTGAGCAGC AATAGGAATT AATCACTGCA GTGCGTGAAT GGAATGTGCT 960
AGGCTCTACC TCAAAATCCT TTTATAAAAA GACTGATATA ATTAAAACCC CAAAGAAATA 1020
TCCAAGGATG CTATATTTGA GAAAATGTGC TGTGAAAGTT TGGAAAAGTG ATTTTTTTAA 1080
AAGGGAAGAC ATGGTAGAAA AGTGTTTCCA TAACTTCTAT ATCATTGGAA ATAGGATTAT 1140
ATTATTACAT CACTGAAGAA TTTATCATAC AAAGGAATTT AAATTGGATT CAATCTTGGT 1200
ACACTGAAAT TTTTTGAAGG CCGAGGGGAT AATCGAGCCT CTCAATTAAG CTGTTTGCCA 1260
TGAAGGGAAA TAACTTCACA GTTAAAATAT CCACCACAAT TTGTAGCAAA GATTACTTTG 1320
GTGATTCAGA CATGTGAATA ACCATGTGAA AAGATCAGAC ATCTGAAGCT TTCAAAATTA 1380
AATGTGAACT ATTGAATTTG TTAAAAAGCA AAAAACCAAC CAAAGAAAAA AAAGAATATG 1440
ACTTCTTGGA ACCTGTTTTT CTATGACTAT AGACGTATTC AGCATCCAAA TCCAACAGCC 1500
CCCCTGTTCC TCTATCACTC TCACATGCCC TCCAAAAGGA GAAGGAAAAG AGAGAAAAGG 1560
AAGGGAGGAA GGAAGGAAGG AAGGAAGAGA GGGAGGGAGG GAGGAAGGGA GGGAAGGAGG 1620
GAGGGAAAGA AAACACTAAC CAGAAGAAAA AGAAGAAAAA TCCCCACTAA CCAGCTCTTC 1680
TTAAAAGGTC ATTAAACAGA TGGCCCAGAA AGGCCTCTCT GACTCTAAGC ACATCACAGG 1740
TAACAAAGTG TTTTAGTTGT TTGAAAGATA ATTTGATGGA AGATCAATTT TTGGACATAG 1800
AGAAAGTGAA AGAGATTTCT TAAACCCACT TGAATTACTG AAGATGAAAG GTTAAAAGCT 1860
TTAAAAACCA AAAACTACAT TAGCAACTGA ACAGTAAATA CCATCAACAG AGACACAAAA 1920
TAATTTAGCA AAACAAATAT TAAATGAAGA CAAGAAAAAA GAATTCATTT CAGAAGCCAA 1980
AAACTTCCTT TTCTTTGTAT TTCAAAATTG ATTTTGCAGT TTTAGACAGA AGTACTAATG 2040
GGTAATTTCT ATTTAATGCT TTCTAAACAC ATGCACAAAA AAATCACTCT CAGCTCCAAA 2100
AGGTCACAGA GATCAAAGCA GGTAGACTTT CTTGGACAGT TTTGCCACCA CTCTACACTG 2160
TATTAGGAGC TGTGAGTGTT TCTACAGTGA AAGATGATAT GATCTGCAGC TTCTTAACCT 2220
TACGTGAATT AGGCTTAAAA CCACACACTA AAAGCCGGTT TCTGTGGCAT TTTGTTTCTA 2280
GAATAGTTGT GTTTCAGGGA AGAACCACTA GGGTGTTGCG AGGCCCAGGT GGTTATATCT 2340
TTTTAATCTA ACAGTAAGAG 2360