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

TagContent
EnhancerAtlas ID
HS056-07062 
Organism
Homo sapiens 
Tissue/cell
GC_B_cell 
Coordinate
chr18:44290130-44293400 
TF binding sites/motifs
Number: 23             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr18:44290487-44290505TCTTCCTTTCTTTCTTTC-6.22
EWSR1-FLI1MA0149.1chr18:44290312-44290330CTTTCCTTCTTTCTTTTC-6.24
EWSR1-FLI1MA0149.1chr18:44290471-44290489TTCTCCTTCCTTCCTTTC-6.46
EWSR1-FLI1MA0149.1chr18:44290308-44290326CCTTCTTTCCTTCTTTCT-6.55
EWSR1-FLI1MA0149.1chr18:44290304-44290322CTTTCCTTCTTTCCTTCT-6.95
EWSR1-FLI1MA0149.1chr18:44290483-44290501CCTTTCTTCCTTTCTTTC-7.02
EWSR1-FLI1MA0149.1chr18:44290413-44290431CTCTCTTTCCTTCCTTCC-7.37
EWSR1-FLI1MA0149.1chr18:44290417-44290435CTTTCCTTCCTTCCTTCT-8.46
EWSR1-FLI1MA0149.1chr18:44290479-44290497CCTTCCTTTCTTCCTTTC-8
EWSR1-FLI1MA0149.1chr18:44290475-44290493CCTTCCTTCCTTTCTTCC-9.72
Hnf4aMA0114.3chr18:44292235-44292251CATGGACTTTGACCAC-6.1
IRF1MA0050.2chr18:44290398-44290419TTTTTCTTTTTCTTTCTCTCT+6.06
IRF1MA0050.2chr18:44290368-44290389TCTTTCTTTCTTTTTCTTTCT+6.14
IRF1MA0050.2chr18:44290388-44290409TCTCTCTTTCTTTTTCTTTTT+6.65
ZNF263MA0528.1chr18:44290429-44290450CCTTCTCCCTTCCCCTTCCCC-6.22
ZNF263MA0528.1chr18:44290413-44290434CTCTCTTTCCTTCCTTCCTTC-6.28
ZNF263MA0528.1chr18:44290435-44290456CCCTTCCCCTTCCCCTTCCCC-6.31
ZNF263MA0528.1chr18:44290475-44290496CCTTCCTTCCTTTCTTCCTTT-6.35
ZNF263MA0528.1chr18:44290436-44290457CCTTCCCCTTCCCCTTCCCCT-6.36
ZNF263MA0528.1chr18:44290416-44290437TCTTTCCTTCCTTCCTTCTCC-6.64
ZNF263MA0528.1chr18:44290456-44290477TTCCCTTCCCTTCCCTTCTCC-6.76
ZNF263MA0528.1chr18:44290463-44290484CCCTTCCCTTCTCCTTCCTTC-6.87
ZNF263MA0528.1chr18:44290459-44290480CCTTCCCTTCCCTTCTCCTTC-7.24
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_56010chr18:44283315-44294827u87
SE_67608chr18:44283315-44294827u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr184429099744292103
chr184429211844292984
Number: 1             
IDChromosomeStartEnd
GH18I046710chr184429058244293280
Enhancer Sequence
GATGCTGGTG CCAGGCTGCA TCATTCTGCC CCATCTCTCT GCCCTCCACT AAGTGAGAAG 60
ACAAATGCAG AAGGCCAGAA AGAGGTGAAC ACAGTGGCCC TGGGCATCAG TTCTCTCCCT 120
GCCCAGACTG GGCTCCAGCT CTGTGGGCTA AGGAGGCCTC CTTTCTTTTT CTTCCTTTCC 180
TTCTTTCCTT CTTTCTTTTC TTTCTTTCTT TCTTTCTTTC TTTCTTTCTT TCTTTCTTTC 240
TTTCTTTCTT TTTCTTTCTC TCTCTTTCTT TTTCTTTTTC TTTCTCTCTT TCCTTCCTTC 300
CTTCTCCCTT CCCCTTCCCC TTCCCCTTCC CTTCCCTTCC CTTCTCCTTC CTTCCTTTCT 360
TCCTTTCTTT CTTTCTCTCT TTTTTTTTTT TTTGATGGAG TCTCGCTCTG TCACCCAAGC 420
TGGAGTGCAG TGGCATGATC TCGGCTCACT GCAAACTCCC CCTCCCGGGT TCAAGTGATT 480
CTCCCGAAGA GGCTCCTTTC AGCATGCCCA GGGTCTGGCC CTCTGAGAGC CTGGGTCTGT 540
AATTCCTATG AGCCTTTCCC CAAAAGCCTG CCCCACAGAG GCTCCCCTGT TGGCCTGATT 600
CCCTCTCCAG AGCTTCTCCA GGGCCATGTT TCCTTTCTTG GGGGCAACAG TACTCTGGGT 660
CCCAGCAACC ACTGGCTGCT ACAAGATGAG GTCCATGCAT TCAGCTTTCT ATCTAACACT 720
TCCCCATCCC CACCCCCAGA CACTGATGGT ACTCCAGAGA ATAGAAGCCC AGGGGGGTCC 780
CTGTGTCACG CACAAACACC TGTTAAATCT CCACTAGCCC TAGGTGAACA GGGAAACTAA 840
TCTGAACACC TAGACTCCTG TCCAGCTTGG TGCAGAGTCT CAGAGAACCA TGGAGTTGTT 900
TATTTATTCC ACACTGGTTA GAGACACCAC TAGCCCATAT AGCGCCTCTG TGCAAATAAG 960
GAAAAAGCAC CATTTTCCCC AGATAAATTA AGCCACATGC ACCAGACACA TGGCTGGTCA 1020
AGTGAGAGTA AGCTGTACTT CAGCCTCACT TGACTGCCTG GCTGAGTATC TTTGTGCAGT 1080
GCCCACCCTG CACAACTGTC CATGACAGCC TGATACCAGA CCATTTAACT TGGTCTCATT 1140
TAATCCTCCC AATAGCCCTA TGAGGCAAGC ATAATTTCCC CCATTTTATA TCTGAGACTT 1200
GAACTACAAG AGGTAAAGTA ACTTGCCCAA GGTCATTCAG CTAGTAAATG GTGGCACTGG 1260
AAAAGAAACC TGAGGACTGT GAGAGCCCGG AACCCCTGCT CTTAACAGTG TCACTGCACT 1320
TCCTCTCCCT GACTCTGACA GCCATCGTTC TCTGGGGGGT TTTCTCAGTC AGCAGCCCTT 1380
CCCCCTCCCA AAGGCAACAG CCCTTCAGTG AGCTCAGCGC TATTTCTAGA GCCAGAACAG 1440
CTGCCGTCTC GAGATAGCAC ACGACCCGTC ACAGCAAACG CACAGAAATC AGTCTGAAAA 1500
TTGCAGCCTG ACAATTCAAA GGACTGAAGT GTCTTCCCAG ATAGGTAGGA GAGAGGCAAG 1560
AACAGCTCAG CTGTTAACAA CTGCGGGTCA CAGCTGTCAG GAGACATGCC ATGGCAGTGG 1620
AGAGCCCCGG CTCCAACCCC TGGCTGGTCC ATGGCCCGGC TCAGCAGCCT TGAACTTCAC 1680
CTGCCCTCTT TGGGCCACAG TTCACTCATC TGTCCCCAGG AATTATCAGA GCTGTTTTGA 1740
GATATCAGAA CTGGATGCTA AAAAGCCTGA TGTTCTCAGT GCAACCCTAA ATAGTCCTGG 1800
GATTAATCTG CCCCAGGTGT GCACCTCACA CCAAGCCTGA GGGTCATTTC TGGCACAGGG 1860
TGGGGGTTGG GGGTAGCAGG GCAAAGCCTG GTGTCTAGCT TCATTCCTCC TTCCCCACCC 1920
CGGAGTTCTG CAGGGCCCCA GATCCAGTGT TTAACATATT CCCTGTGAGA GTATGTACAT 1980
GATGACCTTA TTTTCCAGGC CAGACTAGGG AGCCCTGAAA GGCTTCCCTT TGTAAAATTC 2040
AGCTCAACAG CCAGGAATGC CTCAGTGTGT GAATGCTAGC ACTGGCCAGT GCCCCTACTG 2100
CTTCTCATGG ACTTTGACCA CCATGCCCAC AGGCACCCTA GCCAAGAGAT ACATCCTAGC 2160
TGCCTCCTTC TCCTTCCTTC ATCTTCCGCC AACTCTCACC ACTTCTCCTT CCTGAGTAGT 2220
CCCCATCTCC ACCCCAGTGC CAGGGAAAGG ATTCGGTCTT CTCCCCCCTG GGGGAGTCTC 2280
TCTGTCTGGA ATACTCTTTG CTTTCTTGCT AGTCCCTGCC TACTCATTCA GCAGAGTCAG 2340
CCCAGGGGTC AGCTTCCACT GGCTCCCTTC GTGGCCCTCC CTCCTCTGTG CCTGCAGCCC 2400
CTGGGCACTC CTCCAGACCA GCTCTTATTA TGTGGAATTA CACACAGCTC CTCCATGGCC 2460
TGTCTGCGCT GTTGATGCGT GAGAAGGGTT TTTCTCCTCT TTGACTCATC AAAGATTTAT 2520
AGACCCTCTA CTGTGTGCCA GGAACTGTTT CAGGCCAGGA TGCACTGATG AACTGGCCAG 2580
TGTCCCCACT CTCATGGCAC TTCCACAGGG GCGACAATAA ATGATTCATT CAATATAATG 2640
CCACATAGCC ATAACTCTTC CAAAAAAAAA GCAGGACAAG GAATTGGAGG GTGCCTGGAA 2700
GGATAGTGGG TGGCCTAGGA AGGCCACTCT GGACAGGGGA CATGAATAGA GGCATGGAGC 2760
CCTGTGCAGA TGTGTGGGAA GAACTTCCCA GAGAAGGAAG TGAGTAAATA CAATCACTTG 2820
CTCTGCAGTA GCAGCTGCCA ATGTGGCTAG GCAGGGTTGT GGAGGTCAGA GAGGTGAGCA 2880
AAGCCAAGTC AAGCTGGGCC TGTGGGCCAC CCAGTATCAT GGGGACTCGG CAGAGGAACA 2940
ACGTGATCTG ATGTGGGGAT AAAGGACTGT AAAGGGAGGG AGGGAGAACT ATTGCAGCAT 3000
GAAAAGACAG TCGATTGCAC TAAGGGGTGG CAAAGAAAGT GGGGAGAAGG AGACAGACCC 3060
ATGAAATAGT TTAGGAATGG AACCAGCAGG ATGCATTGAT AATTTAGAAA GTGAATAAAT 3120
CAACAGTAAC TCCTAGGACT TCAGCTTGAA CAACTAGCGG GATGACATAA CCATTTAAAG 3180
GTTAGAGAGA TGAACAGGTT TGGGGTGTTG GGCCCTGTGA AGCTTCCTGT GCCCTCAGAC 3240
ATCTAGAGGA GATCACAGGT AGGCAGTCAG 3270