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

TagContent
EnhancerAtlas ID
HS049-04062 
Organism
Homo sapiens 
Tissue/cell
Fetal_spinal_cord 
Coordinate
chr19:33920870-33922420 
TF binding sites/motifs
Number: 34             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr19:33921746-33921765CTGCCACCAGAGGTCGCAA+6.4
EWSR1-FLI1MA0149.1chr19:33922071-33922089GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:33922088-33922106GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr19:33922043-33922061GAAAGGGAGAGAGGAAGG+6.11
EWSR1-FLI1MA0149.1chr19:33922152-33922170CGAAGGAAGGAAGAGAGG+6.52
EWSR1-FLI1MA0149.1chr19:33922083-33922101GGAAGGGAGGGAGGGAGG+7.08
EWSR1-FLI1MA0149.1chr19:33922015-33922033GGAAGGGAGGAAGGGAGA+7.21
EWSR1-FLI1MA0149.1chr19:33922047-33922065GGGAGAGAGGAAGGAAGG+7.26
EWSR1-FLI1MA0149.1chr19:33922112-33922130GGAGGGAGGGAAGGAGGG+7.36
EWSR1-FLI1MA0149.1chr19:33922051-33922069GAGAGGAAGGAAGGAAAG+7.57
EWSR1-FLI1MA0149.1chr19:33922011-33922029TGAAGGAAGGGAGGAAGG+8.05
EWSR1-FLI1MA0149.1chr19:33922079-33922097GGAAGGAAGGGAGGGAGG+8.13
EWSR1-FLI1MA0149.1chr19:33922055-33922073GGAAGGAAGGAAAGAAGG+9.09
EWSR1-FLI1MA0149.1chr19:33922067-33922085AGAAGGAAGGAAGGAAGG+9.09
EWSR1-FLI1MA0149.1chr19:33922059-33922077GGAAGGAAAGAAGGAAGG+9.17
EWSR1-FLI1MA0149.1chr19:33922075-33922093GGAAGGAAGGAAGGGAGG+9.42
EWSR1-FLI1MA0149.1chr19:33922063-33922081GGAAAGAAGGAAGGAAGG+9.47
SOX10MA0442.2chr19:33922347-33922358AAAACAAAGCA+6.02
ZNF263MA0528.1chr19:33922053-33922074GAGGAAGGAAGGAAAGAAGGA+6.06
ZNF263MA0528.1chr19:33922052-33922073AGAGGAAGGAAGGAAAGAAGG+6.12
ZNF263MA0528.1chr19:33922020-33922041GGAGGAAGGGAGAGAGGAACA+6.27
ZNF263MA0528.1chr19:33922072-33922093GAAGGAAGGAAGGAAGGGAGG+6.76
ZNF263MA0528.1chr19:33922017-33922038AAGGGAGGAAGGGAGAGAGGA+6.85
ZNF263MA0528.1chr19:33922101-33922122GAGGGAGAGAGGGAGGGAGGG+6.8
ZNF263MA0528.1chr19:33922056-33922077GAAGGAAGGAAAGAAGGAAGG+6.93
ZNF263MA0528.1chr19:33922068-33922089GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:33922012-33922033GAAGGAAGGGAGGAAGGGAGA+7.02
ZNF263MA0528.1chr19:33922085-33922106AAGGGAGGGAGGGAGGGAGGG+7.05
ZNF263MA0528.1chr19:33922076-33922097GAAGGAAGGAAGGGAGGGAGG+7.19
ZNF263MA0528.1chr19:33922080-33922101GAAGGAAGGGAGGGAGGGAGG+7.38
ZNF263MA0528.1chr19:33922089-33922110GAGGGAGGGAGGGAGGGAGAG+7.43
ZNF263MA0528.1chr19:33922093-33922114GAGGGAGGGAGGGAGAGAGGG+7.4
ZNF263MA0528.1chr19:33922097-33922118GAGGGAGGGAGAGAGGGAGGG+7.96
ZNF263MA0528.1chr19:33922109-33922130GAGGGAGGGAGGGAAGGAGGG+8.31
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr193392122033921907
Number: 1             
IDChromosomeStartEnd
GH19I033430chr193392150933922611
Enhancer Sequence
ACAATTAATC TTGAGGCCTG GGTGGGCACA CCGGCACTCA TGGTTTGGGA GGAGGGGTGT 60
CCTGCACGCT GGCTGAGAAC ATGGCTTCTG GAGAGAGGCC ACCTGGCTCC TCTAAGACCC 120
ATCTGTCTAC TGTGGGGTCT CTATAATGCA GAGAGGATGC CACACTCCTC TCCGCTCCCC 180
CTCACGGGAT TAAATGAGAA CATCCCCGGG AAGGACATGG TATCTGCTCA CCAGACACTA 240
ACCCAGCCCC AGCCGTGAAG GGAGAACAAC TTTTCTAGAT GGCACTGGGC TTTGGGCATC 300
AACATTTTTC CAGCAATTCC ATTTGCAGGA GTTTACCCCA AGGACACGGT CAGTTTGACA 360
CCCGAGAGAC GGCGAGGTAG GGTTGACGGT CGAAGTGTCG TTCACACTGG GAACCACCTG 420
GCTTCCGGGG GCAGTCTGGG TAAGTGGATT ATGATGCAGC CCCAGTGTGC CCCAGTTCAC 480
TGCCAGGAAG AGACTTCTGC TGCAAAAACT CTGCCCAGTG TGAGCCCAGC AGATCAAAGC 540
CCGTCTGTCT GTGCCCCAGA GAGACCGGAA GCCTGTTTGC TACAGCAATA AGGTTTTGTG 600
TGCCTCTGCA TCAAAGGGTT TTTTTCCTAT CTTGTTTATA ATGTTCTGTA CTGACTGGAT 660
TTCCTACTGG CATATGTATC TTTTTATCAG AGTAAAGCTA TTTTCATTTT GAAAACACTT 720
TTGGGAAGAA ATAAAAGCTA CCTGTCAAAG ACCTGCTCCC CTCGCCCCAG CCTCGCCCCA 780
CTGGCCCCAG GGGGCTTCTT GTCCTGATGT GTTCTGCCCA GTGGACACAG CGCACACTCC 840
CCAAGCACAG CTGCCACCGA GGACGACACT GGGAAGCTGC CACCAGAGGT CGCAAGTGCA 900
CGCCGTCTGC CACGCACACA GAGCTCCTTG AAAAACCTTC AGCCTGGCTG AAGGAACCAC 960
AGTGTATCTC TGTTTTGATA CCATTGTTGT GGACAAAGTA AAAAATAAGC AATCCAGCCA 1020
GGTGCTGTGG CTCAGCACTT TGGGAGGCTG AGGCAGGAGG ACTGCTTGAG CCCAGGAGGT 1080
CGAGGCAGTG AGCTATGATC GCACCACTGC ACCCCAGCCT GGGCAACAGA GCAAGATCCT 1140
ATGAAGGAAG GGAGGAAGGG AGAGAGGAAC AGAGAAAGGG AGAGAGGAAG GAAGGAAAGA 1200
AGGAAGGAAG GAAGGAAGGG AGGGAGGGAG GGAGGGAGAG AGGGAGGGAG GGAAGGAGGG 1260
CAATTCAAGC CCAATTCCTT CCCGAAGGAA GGAAGAGAGG GACGAAAAGA AAGAAAAGCA 1320
ATTCAAGCCC AATTCCTCCC TGACTCTATC AGGAAACTCT ACCATGGGTT GAAATCACCC 1380
AAAATCTGAA TGTCCAGGTC CCCGCCGGAG GCCAGGGCTG GGGGCCCATC TTCATCATCC 1440
CAAAACTCAT GTGGGAAATT TCCCCAAGAG GAGACAGAAA ACAAAGCAAA GATTTCCTCT 1500
CTTCATTCCG CCCAAGACAA AGCATCTGAA ATTCCACTCT CGATGTTTCC 1550