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

TagContent
EnhancerAtlas ID
HS050-34037 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr19:42431320-42434260 
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr19:42432893-42432913GGAGTGGGGGTGGGGCGGGG-6.02
RREB1MA0073.1chr19:42433766-42433786CCCCAACCCACCACCCCCGA+8.42
ZEB1MA0103.3chr19:42432023-42432034CCCACCTGCCC+6.14
ZNF263MA0528.1chr19:42432631-42432652TCCTCCTGCTCCTCCTCCTCC-10.05
ZNF263MA0528.1chr19:42432656-42432677TCTCCTCCTCCTCCCTCCACT-6.26
ZNF263MA0528.1chr19:42432956-42432977TCTCCTCCGCCCCGCTCCTCC-6.28
ZNF263MA0528.1chr19:42432652-42432673TCGTTCTCCTCCTCCTCCCTC-6.42
ZNF263MA0528.1chr19:42432619-42432640TCTTCCTCCTCTTCCTCCTGC-6.61
ZNF263MA0528.1chr19:42432649-42432670TCCTCGTTCTCCTCCTCCTCC-6.7
ZNF263MA0528.1chr19:42432940-42432961TCCTCTCCCCTTCCCTTCTCC-7.15
ZNF263MA0528.1chr19:42432661-42432682TCCTCCTCCCTCCACTCCTCT-7.2
ZNF263MA0528.1chr19:42432610-42432631GCCTTCTCCTCTTCCTCCTCT-7.46
ZNF263MA0528.1chr19:42432640-42432661TCCTCCTCCTCCTCGTTCTCC-7.54
ZNF263MA0528.1chr19:42432613-42432634TTCTCCTCTTCCTCCTCTTCC-7.58
ZNF263MA0528.1chr19:42432943-42432964TCTCCCCTTCCCTTCTCCTCC-7.64
ZNF263MA0528.1chr19:42432646-42432667TCCTCCTCGTTCTCCTCCTCC-8.4
ZNF263MA0528.1chr19:42432643-42432664TCCTCCTCCTCGTTCTCCTCC-8.58
ZNF263MA0528.1chr19:42432625-42432646TCCTCTTCCTCCTGCTCCTCC-8.94
ZNF263MA0528.1chr19:42432616-42432637TCCTCTTCCTCCTCTTCCTCC-9.03
ZNF263MA0528.1chr19:42432622-42432643TCCTCCTCTTCCTCCTGCTCC-9.18
ZNF263MA0528.1chr19:42432628-42432649TCTTCCTCCTGCTCCTCCTCC-9.18
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_60313chr19:42431637-42456169Ly4
SE_60575chr19:42431108-42443012DHL6
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr194243166242432200
chr194243379542434249
chr194243225042433692
Number: 1             
IDChromosomeStartEnd
GH19I041929chr194243410142434250
Enhancer Sequence
GAGAGACAGT GAGGAGAGAC CCAGCCAGGG GAGAGATAAC AGAAGTGGCC CAGCAGGGCC 60
CTGCGACAGT GGTGGAATGA TAGAAAGGGT GTCCCAGAGG GCCCCGGCCC CACGAAGGTC 120
AGGGCCAGGC CTGTACTCCT TGCCCCGAAG TGTGCAGACC CCAGAATTGG CCCAAATGTC 180
CTTCCCACAG ACCCTGTGAC CCCTCATACC AAATATCCAG ACCCCAGATA TCCAGATCCA 240
AATTCGCAGA CCCTTAGCTT TGAACTCCAA CTCCAAATCC AGACTTCTGG CCCCCTCAAG 300
TCCAAACTCC TATGCTGATC CCCAGTCCCA GATATCCACA CCCCCAGTCC TGACTCCCAG 360
CCCCAGTCAG CTCCCAACCT CAGATATCTA GATCTTCCGC CCCAAGTGTC CAGTCTCTTG 420
GCTTTGAGCC CCTAGGTCCC AAATATGCAA GCCCTCAGCC CTGACCTCTA AACCCCACTC 480
AGAATCTAGC CCCAAATATC CAGACTCCTC AGCCCCAAAC ATCCAAATCC ACCTTCAGGT 540
CGGCCACCAA CCCCCGTTCC CAGATTTTCA GTCCAGTCTC TTGCAGACCC CATCTCCGTG 600
GCTCTCACTC GCTCTCCCTC CCCGCCCCCA AATCTCGCAC CCCTGTCCCG AGGCCGCACC 660
TCTAGCGCTA CCCGCCTCCC ACCTTCCCAG AGTTGGGCGC TGCCCCACCT GCCCCTTACA 720
GCCGGGGCGG ATGACCCCAT CCGCCTACCC CTCCACCGGC TCGGAGGCCC AGCTTCTCAG 780
GCCTCCCGGG ACCACCCCCG CGCCCGCCCC CTCCTGGGGC GGGAATCCCC GCCCCCTCCC 840
CGCCCCTGCG CCGGCCGCGG CGCTCACTCA CTTTCTGGGC TTTTCGCATC CGCTCCGGTC 900
CGGGGAGAAG TGTTTAAAGT TCGGATCCCG CAGCCATGGC CCCCGCGGCG TCCTGGGGAG 960
GGGGCACCGG GGCGAGGGGC GGGGTGGGGG GAGATGCCCG GAGCCCCGGG GAGGCAGAGA 1020
CCCAGAGGAC GAGGAGAGGG AGTCTCTGAG ACGCCGGGAC AGGAGAGACT CAGAGACGGA 1080
GAGACAGCCA AGGAGACAGA GACGGGGAGA CGAGCAGAGA CGGGGAGATG CAGAGAGGGA 1140
GAGAGACAGC GAGATAGACG CGCAAAGAGA GCAGAGACGG GGAGAGCTGA GGACGGAGCT 1200
CCGGGCTGGA GCTCAGCACA GCGAGCGCGG GCGGGCGCGC GCCGGGGACA GCCTGGCCGG 1260
CTGGGGGCGC GGGGCGGCCC TGCCTCCTGC GCCTTCTCCT CTTCCTCCTC TTCCTCCTGC 1320
TCCTCCTCCT CCTCGTTCTC CTCCTCCTCC CTCCACTCCT CTGCGCGCCG CGCGCCTCCC 1380
GCCCTCGCGG CCGCCCGGCC GGGCTCGGCT CGCAGATATA TGGAGGCGGC GGCGGCGGCG 1440
CGGGGGAGGG GGCGGGGGCG CGATCGATGG AATATAATTT TCCTCAAACT CGGAAAATAA 1500
AGTTCAGAGC TGATCAAATT TGAAAACAGA TGTCGAATCG CGACTCTAAA TAAGGTTCGA 1560
TCCCGGGACT GAGGGAGTGG GGGTGGGGCG GGGGTGGGTG GAGAGGTGGA GAGACCCCCC 1620
TCCTCTCCCC TTCCCTTCTC CTCCGCCCCG CTCCTCCCTA AGTGGACGCG CGGACAAACG 1680
GACAGGCGCG AGGTGGAGGT GGCGACGATG CGTCCAGGAC CCCTGCTGGA CACGCAAGCC 1740
TGGACCGGGA CTGGAACACG GACCCGCACA CACGCAGCCT GGATAGGAGA TACACGGACA 1800
GAGGGACATA TGGATACAGT AAGACAGTGC AAACACACAC TCAGGGACAC ACAACCCTAC 1860
AGAGAGACAG ACACAGACAC ACACACACAG ACCTGCCATC TATACACGCA GCACACACAT 1920
GCGGACCGTA ATACAGGAAG TGGAAACACA ACCGGTACAC GGAGACATTC AGGCACACAC 1980
AGAGAAACAT ATGCACAAAC ACAGCCTGCA CACCACACCT TCCCCAACCC ACAGCCACTC 2040
CCTGATCCAC TGACCCACAA ACTGGACACA AAGACAACCA GATGCACACA CAGCCACACT 2100
CCACTCCCAA CACACAGCCT GGACACACAA GCCCTCACTA ACACATAGGC AGAACCCAGG 2160
GCTGGCACAC TGACACTCCC CTTCACACTC CCACAAGGTC ACAGGCACAC ACACGCACAC 2220
CTACAGTGAC AGGAAAGGGC CCTGCCCAGC CAGATCTGCT CCCATTGAAA TAACAAGTCA 2280
ATATCGACCA GCCTCAGGGC GGGTCAGACC CACAGTTCAG CTCCCGGCCG GCCGGACCTC 2340
CTGGCCCAAC CTGACCCTCA CCCTCACTGT CTACCCTCCT ATTCCCTCCC TTGCCCCTTG 2400
CCCCTCGCCC CTTGCCCCTC ACCCTGCCCT CTCTCCCGCT TCCACTCCCC AACCCACCAC 2460
CCCCGACTTT TCTCTCCCAT TCCCAGGTCA GGCTCCGCCC CGCCAAGTCC CACACCACCT 2520
TCTCTGGGGA AAGGCAGCTC TCACCTGGGC AGCCCCTGGA GGCTTCTACC CCTAGAGGGG 2580
AAAATAGGTC TCACGGCAAG ACAGCAGTCC CCAGGTGGAT ATTCAGGGGC CAGGACAGCT 2640
CTGTCGGATC TCACCAACCC CACCAGCGCC CAGGTGCTGA GACCGAGGTG CTGAGAGGCT 2700
AGAAGAGAAC TTCAGCCCTG CCTGACAGAG AAGGTTCAGC CTCACTCCCG CTCACCACTC 2760
ACTCAGGCAA GTCGCTAAAC ATCCCCGAGC CTCAAGTTTC CTCATCTGCA AAATGGGACA 2820
ATAATGACCT CCCTCCTAGA GTGGTTGGGA AGGTTAAACC GCAGGGCGCA TGGAGCACAG 2880
CTGGTACTGC ACCAAGTACC AAGTAAACAC GCATTTGCTG TGAGCTTGCT GCTTCCGAAT 2940