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

TagContent
EnhancerAtlas ID
HS197-10874 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr19:48231050-48234220 
Target genes
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr19:48231818-48231839TCTTTCTTTCTTTTTTTTTTT+6.25
IRF1MA0050.2chr19:48233139-48233160TTTTACTTTTTCTTTTATTCT+6.26
IRF1MA0050.2chr19:48231804-48231825TTTCTCTTTCTTTTTCTTTCT+6.27
IRF1MA0050.2chr19:48231774-48231795TCTCTGTTTCTCTTTCTCTCT+6.42
IRF1MA0050.2chr19:48231792-48231813TCTTTCTTTCTCTTTCTCTTT+7.75
IRF1MA0050.2chr19:48231798-48231819TTTCTCTTTCTCTTTCTTTTT+7.83
KLF16MA0741.1chr19:48233571-48233582GCCCCGCCCCC+6.02
KLF4MA0039.3chr19:48233921-48233932GGAGGGTGTGG-6.32
KLF5MA0599.1chr19:48233571-48233581GCCCCGCCCC+6.02
NFYBMA0502.1chr19:48232117-48232132CACCCAGCCAATCAG+6.18
SP1MA0079.4chr19:48233568-48233583CAGGCCCCGCCCCCA+6.56
SP4MA0685.1chr19:48233568-48233585CAGGCCCCGCCCCCAGC+6.4
Stat4MA0518.1chr19:48231548-48231562CCTCTTCCTGGAAA-6.08
ZNF263MA0528.1chr19:48231733-48231754CTTTCCTTTCCTTTCTTCTCC-6.03
ZNF263MA0528.1chr19:48233491-48233512CCCTCCCGCCTACCCTCCTTT-6.1
ZNF263MA0528.1chr19:48233176-48233197CTTTCTCGCTCTGCCTCCTCC-6.39
ZNF263MA0528.1chr19:48232756-48232777TGGGGAGGGAGAGGAGAAAGG+6.97
ZfxMA0146.2chr19:48233568-48233582CAGGCCCCGCCCCC-6.19
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_00405chr19:48230883-48234933Adipose_Nuclei
SE_03083chr19:48231362-48231780Bladder
SE_03083chr19:48232106-48233503Bladder
SE_26919chr19:48231327-48231819Esophagus
SE_26919chr19:48232018-48234409Esophagus
SE_30773chr19:48232024-48233662Fetal_Muscle
SE_42926chr19:48231259-48234475Lung
SE_45513chr19:48231970-48233389NHLF
SE_46861chr19:48232166-48234149Ovary
SE_47852chr19:48232120-48233927Pancreas
SE_66815chr19:48232043-48233375Jurkat
SE_66815chr19:48233707-48234177Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194823158348231681
Enhancer Sequence
ACATAAAATA ACAATGAAGG CTGGGTGCGG TGGCTCACGC CTGTAATCCC AACACTTTGG 60
GAGGCCGAGG GGGGAGCAGA TCACTTGAGG TCAGGAGTTC GAGACCAGCC TGGTCAAGAT 120
GGTGAAACTG CGTCTCTACT AAAAATACAA AAATTAGCCA GGTGTGGTGG CGGGCACCTG 180
TAATCCCAGC TACTTGGGAG GCTGAGGCAT GAGAATCACT TGAACCCGGG AGGCAGAGGT 240
TGCAGTGAGC TGAGATTGTA CCACTGCACT CCAGCCTAGG CGACAGAACG AGACTCTGTC 300
TCAAAATAAA AAAAAAAAAA AAGATGAATT TATTACATCT TAGGCGCTTC ACAGCACCCG 360
TCTCCCATGA CTCTTGTTTG ATTGTGGCCA CAGATTGTCC CCTTCTCTCA CTCCTTTCCT 420
CTGTCCTCAT CTCCCATTCC CTTCCCAGCG TCCCCTGCAC TTCACGCTGG TGGCCTCAGT 480
CCTGTGCACT TGCTGCTCCC TCTTCCTGGA AACCTCTTCT GCCTTCTTCC CCCTCCCACC 540
TGGCCATCCA CAAGGCTCAC TCCCTCCTCA CCCCTTTCAA GACTCTGCTC AAATGCTCCC 600
TTCTCAGGAA GGCTGTCCAT GCCCTCCTTT GAATGAATAT AACTTCCCCC ATATGCGTCC 660
TTCTTTACCC TAACCCTGTT GTCCTTTCCT TTCCTTTCTT CTCCTCTCCT CTCCTTTCTC 720
TCTTTCTCTG TTTCTCTTTC TCTCTTTCTT TCTCTTTCTC TTTCTTTTTC TTTCTTTCTT 780
TTTTTTTTTT TTTGAGACAG GGTCTCCCTC TGTTGCCCAG GCTGGAGTGC AGTGGTGCGA 840
TATCAGCTCA CTGCAACCTC CACCTCCCGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCCT 900
GAGTAGCTGG GGTTACAGGC GTGTGCCACC ACACCCAGCT AATTTTTTGT ATTTTTAGTG 960
GAGACGGGGT TTCACCATAT TGGTCAGGCT GGTCTCGAAC TCCCGACCTC AGGTGATCCG 1020
CCCGCCTTGG CCTCCCAAAG TGCTGGGATT ACAGGCGTAA GCCACCACAC CCAGCCAATC 1080
AGGGCTCTTT GAATTCCTTC ACTGATTTAT CCCCAGTGCC CGGAACAGAA TTGGTGCTCT 1140
GTAAATATTT ATTGAATGAA TGACATTGAA CAAACAGTTG CATTGAACAA AATCTCCTCT 1200
ATGCCTGGCC TGGTGTTGGG TGGTGCAGGA GACACAACAG TGACCACGAT GGTTCCAGTC 1260
CTGTCCTGCT GGGGCTCCCA GTCCTAAATA ATGAAGGCAG TTCCAGGGCT CAGTCCTCAC 1320
TGGGGCTCCT GGAGAGGAGA CAGATCCATC CCCAGGCACC GATGACCCAG TGTGGTCAGA 1380
GCTGGGGCGG GGTAGCTGGG GCAGGCAGAG AGGGCTTCTT TGGAGGAGAG GGCATCTGAG 1440
GGGAAATGTC AGTGTTGAAC CCAGTGTAGA CAGTGTGCTA ACTCAATTAG AGGCTGAGGA 1500
TGTGGCTGAG ATCAGAGGTG GTGTGGGCTG TGTCCGGGAA TCTGTGCTTT GTCCCTAGGG 1560
CACTGGGGAG CCATGAAAAA GTTCGGAGCA GGGAAAGGAG ATAATTAGAC TCAAGCTACC 1620
TTTTGGAGGG TGGATTCAAG GCAGGAGAGT CTAGGAGCCT GGAGACCAGG CAAAAGGCTT 1680
GGAGGTTCCT GGATCAGGAC AGGCCTTGGG GAGGGAGAGG AGAAAGGAGA GCGCGGGTTT 1740
CAGAGCGATT TTGGATGTCA GATGGAACTT TCTCAGGGGG AGGCTGCCAG GGTGGAGGCG 1800
GGGCAGGAAG CTGGGCAGGC AGGGAGGCCA AGAAGGTTCT AGGGGGTGGA GGAGCCTGAG 1860
GTGTTGGTTT AAGGAGCAGC GAGAGTGGGT GAGTCAGAGC CCCCACCCCC ACCCCAGGAA 1920
TCCTCCTTCG GAGGGAGCGG CCCACTGTGG ACCAGGCTGC CACTCCTGGA ACCTTCGGAA 1980
TTCACCTTGC GCTCCTCTGC CCAGGCGGCT CTGCAGTGTC TCTCTCTCTC TTTTTCTGTC 2040
TCTATGTCAG TCTCCTTTCT ACCTCTCTCT CAGTCTCTTT CTTCTCCATT TTTACTTTTT 2100
CTTTTATTCT AACTCCCTTT CCTTTTCTTT CTCGCTCTGC CTCCTCCTGT CTCTCCATCT 2160
CTCCCCCGCT CCGCCGCCGC CCTCTCTCTG TCTTCCTCCT GGTCTTGCTT AGACTCCCCC 2220
AGGTTCGTTC CCGCGGGTCC CTTGGCGGGA GCTGGAGCAC AAGGCCCAGG GACAGAGGGG 2280
TGGGTCCGGG CCAGACACCT GGTGCCCCCG CCGGGCTGGG GGCGGCTCCG GAAACCCAGA 2340
CAAACCCCGG AGTCAGGGAC CCAGCCCCGG CCCAGCCCGC CCTCTCACCT TATCTCTTCC 2400
TGGCACCTTC CCCTGCTTCC TCTCTGGAAA AGCCATCAGC GCCCTCCCGC CTACCCTCCT 2460
TTGGTCCCTA CGGAGCCGCC CTTCGGCCCT GCCCCCTGGC TCCATTGGCC CGCTCTCACA 2520
GGCCCCGCCC CCAGCCCGGC CACACCCCTG CCCTGATTGG TCCTTCAGAC CATTAGGCAC 2580
TCCCTCCCCC TCTTCCTGCA GGTTCATCCA TGGCTCCCCA GTGCCGTTCA GGACACAGGA 2640
GCATGGGATT TAGGGTCCGC TGTGACCAAG GCTCACTGCC CCTCCTTTGC CCCGTGTCGC 2700
ACCCCCACCC CTGCTCCTCA CATATGAGTC CGCCACACTT GGTCGTCACC AACAATAGCC 2760
ATACTGTTAA CCTCCCCTCA TGCTCTCCTC CAAAGATACC AGGCCTTCCT GGACTCTCTG 2820
GGAGGAGGCA TTCACCCTCC TCCCAGTGCC TCAGTTTCCC ATCTGTACGA TGGAGGGTGT 2880
GGACGAATCC TCTGGCTCTA AGTCCTTTGG CTGAAGTGAT AGCTGTTAGA AGGGGAGATT 2940
TTATGATGCT GTGATACGTA AGGCCAAGAT CTTGGGAGGG TCTGATTCTA TAGACGCCAA 3000
GATGCCCTGA ACCTTCAGAC CACATTCTCT GCAGTGGCCC AGTGACATTC ATTCAGCAGT 3060
TGCCGATCGC ATGTGGTACT CCTCTAGGCT CTGGGGATAC AGCAGGGAAC ACAGATAAAT 3120
TCCTTTTCTC ATAGAATTAC TTTTTAGTGG GGAAGCAAAC ATTAAACAAA 3170