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

TagContent
EnhancerAtlas ID
HS158-00906 
Organism
Homo sapiens 
Tissue/cell
Pancreas 
Coordinate
chr1:21949040-21952100 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1318236chr121952024hg19
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:21950675-21950693GGGAGGAGGGAAGGAGGG+7.36
HNF1AMA0046.2chr1:21950208-21950223TTTTAATAATTAACA+6.05
HNF1BMA0153.2chr1:21950209-21950222TTTAATAATTAAC-6.14
KLF16MA0741.1chr1:21949073-21949084GGGGGCGGGGC-6.02
KLF16MA0741.1chr1:21949134-21949145GCCACGCCCCC+6.62
KLF5MA0599.1chr1:21949074-21949084GGGGCGGGGC-6.02
KLF5MA0599.1chr1:21949107-21949117GGGGCGGGGC-6.02
KLF5MA0599.1chr1:21949112-21949122GGGGCGGGGC-6.02
NRF1MA0506.1chr1:21949176-21949187GCGCCTGCGCG+6.14
SP1MA0079.4chr1:21949131-21949146GAAGCCACGCCCCCC+7.49
SP3MA0746.2chr1:21949133-21949146AGCCACGCCCCCC+6.74
SP4MA0685.1chr1:21949131-21949148GAAGCCACGCCCCCCGG+6.42
SP8MA0747.1chr1:21949134-21949146GCCACGCCCCCC+6.44
ZNF263MA0528.1chr1:21949557-21949578TTCCTCCTCCTCTCCTCCATC-6.05
ZNF263MA0528.1chr1:21949554-21949575CTTTTCCTCCTCCTCTCCTCC-6.16
ZNF263MA0528.1chr1:21949549-21949570TGTCCCTTTTCCTCCTCCTCT-6.65
ZNF263MA0528.1chr1:21949564-21949585TCCTCTCCTCCATCCTGCTTC-6.73
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_00987chr1:21949130-21950367Adrenal_Gland
SE_00987chr1:21950822-21951982Adrenal_Gland
SE_04282chr1:21949177-21952719Brain_Anterior_Caudate
SE_05416chr1:21949072-21952361Brain_Cingulate_Gyrus
SE_06618chr1:21949350-21952242Brain_Hippocampus_Middle
SE_08200chr1:21949387-21953199Brain_Inferior_Temporal_Lobe
SE_31655chr1:21944407-21954108Gastric
SE_41934chr1:21949180-21952051LNCaP
SE_47603chr1:21949067-21950213Pancreas
SE_47603chr1:21950289-21952007Pancreas
SE_65280chr1:21949125-21951967Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12194920021950637
Enhancer Sequence
CTGCGATGGG CTCGCCCCAC GGCGGGGCCC GGAGGGGGCG GGGCGCCAGG TACGGGCGGC 60
ACGGCGCGGG GCGGGGCGGG GCGGGGGCGC TGAAGCCACG CCCCCCGGGC GGCCCGGCCC 120
GCGGCCCCGG GACACCGCGC CTGCGCGTTC CGGCCCGAGC GCTAGAAGCT TTGGGTGCGT 180
CGGGCTCCCC GAGGGGGCCC CCCACTCGGT TCTCCCCAGC GCGCCCCCAC CTCACTTTCT 240
CCATCTTCCC AGGCTCTGGG TACCCCGCCT CGGCATCAAG GACAGGGTTG GGTTACCTTG 300
CAGACAGAGG GCTTTTCTTG AGCACCTACT TAATGCTGGG CCCTTCGCAT GTGTCGTAAT 360
CTCGTCACAG CCCAGGAGGT ACAAATGTCA TCTCCATTAT ACAGATGAGA AGCCGGTTCC 420
AAGAGGTGAA ATAGCTTGCC CGAGACCACA CAGTCAGGAA GAAGTCAAAG TGGAATCCAG 480
AGAAAGGCCT GGTGCTACTC TTTGGGGTCT GTCCCTTTTC CTCCTCCTCT CCTCCATCCT 540
GCTTCCCATG CCTCACAGTG GCTGGCCTGC TCCGTCCCTT CCCCCGCCCT AGCTGCCCCA 600
GATCCTGGGG GAGATGGCCA CAGCACCTAG GGAGGGGCTG CCAGGCCCGT GGTATGGAGG 660
AAAGGACCCA AGTAGATTTT GGGACATGTG GATTCTAGCT ACAACTTGCT GAGTGGCCTT 720
GAGTGAGTCC CTGCCTCCTC TCTGGACCTC AGTTTCCCCA TCTTTAAAAT ATAAGGACTC 780
TGTAGGCCCT TCCAGCTGGC TCTGCAGTGT GTCCCTGGCC TGGTATAGCC ACTGTACAGC 840
AGGGACAGGG ACAGGGCCTT GCTACCACTT CCTCCAGACA GATGTTGGGA ACACAGCAAA 900
TGCTTCCTGA ACTGTGGCCA AGCAGACACA GCTGCTTTGG ATGTTGCGGG GGCAGGGCTG 960
CCCACCAGCT CAGAGCCATA CCTCTGTTCA GCTTCCTGAA AGAGCTGCCA GTGGCTGCCC 1020
ACCACCCTCC AGCCCCAGAA CTAAGGGCTC CTGGAAGGAA AGCACTGTGC CCTCCCTTTC 1080
CCCCTAGACC TGGCCTTGAA TCAGGTTTGG GCCTGGAGAG CCAGCAGGAA CTCTGGAGAT 1140
GGGTGTTCCA GACACGGTGT AGCTTTGGTT TTAATAATTA ACAACAGCAA ATATTGATTT 1200
ATGCAGCCAC TTCCAGGCCT GAATGCTTCC GGGCACCCAT CGAAATCCAG CCAGAGAAAC 1260
ATCCATTCCC ACACTGCCCC CGGGGGAGGC GAGACCTGCT CACAGCACTG GAGATGGCTG 1320
TGTGCCAGGT GGCATGGAAG GTGTGTGCAC ATATGCGTGC AGCCATGTGT GCGTGTGTGT 1380
GAGACTCCAC GACCGGATGT GGCTGTATGT ATGTGGGCAT ACTGTCTTTC TGTGTGTATG 1440
GGAATGCCTT GGTATGGGAA TTTGTGTTTG TACATGTGTA TCTCATGCAT GTGCAAGTCT 1500
CTGAATATAT TTACAGACCA GTGGCTGTGG CTGTGTGTTT TGTGTCTGTG ACTCTGTCCC 1560
CATATGTAGG TGTGGGTAGG CTGTGTATGT ACGTGTGTGC AGGTTTCTGA ATCCCCGAGT 1620
GGAGAAACCC CTGTAGGGAG GAGGGAAGGA GGGTCCTGGG TAGCTCGATG CCTGTACAAA 1680
TGTGGGGCCT GAAGGGAGGA GAATGTCCCT TCTGGGTGCC CTGTCCAGCC CTGGGAATGT 1740
AATGACGCTG ATAAGAGCTC AGCTTCCTAA TTTCTACTTT CCAAAGTACT TTCACCCAAT 1800
TGCAAGCTGG CAAGGCAGGT AGAGAAGAAA CTGTCACCTC TGTTTTACAG ATGAGGAACC 1860
TGAGGCCCAG AGACGGGCAG GGATTTGCCC ACTGGCAGAG GAAGGTCACC TGCCCTTCAG 1920
ATGGATGCCA TCCATGTTAT AAATGTGCAC AGAGCTAGGG GCACCAGGGG AGGGGAATGG 1980
AGAATATGTC ACAGGCCTGT GTTCCCTCAG CCCAGCACTG GCTTGCTGGA GACCCCAGAT 2040
GAATCATTCA GTCTCTCTAG CCCCTGGTTT CCTCTCCTGT CAAAGGAGGA TGGTCCACAG 2100
ACTCTTGATT CTGAGGTGGG GGTGGGCTGT CGGGAAGGGA AGGTTCAGAG CCCGCTGTCT 2160
GAGCTGTGTT GGCACAAACG GAGGCTTCTA GCCAGACTGG GTGGAAGCCA GGAAGCCCGA 2220
GGGGAGGCAG CTTTTCAATA ATCCGAGAAG GCCAACCCCA GGCTGTCTAG CACGCAGGGC 2280
CCAGGGCTAT GGGCTGCTCT CTCTCTCTCT CGTCTCCTGA TGGGAAGACT GAGGCCCAGG 2340
GAGGGGAAGC TGTGGTCCGA GGGCATACAG CCCTTGGTGA GAACCCAGGG CTCCTCCTGA 2400
GATGCTCAGG GGAAGAGGGA CTGGGAGCTT CATTCATGAA CCCAGCTGTC AAGTGAGGGC 2460
TGCCATTGAG TCTCTCCCTT CCTGCCAAGC CCCGGATCCA CATGCCCCAG TCTTGGGCTG 2520
TTGCCCAGAC AGAGAAAACA GGAGTCAGTC TCAGGAATCT CCTGCTGCTG CTCCCAGCAG 2580
CCCCACGTGG CACCCCCATG AAGGTGGTGG CCCCACATAT GGACACCATT CCTTGGCCAT 2640
CTGCCCTCCC AGCCTAGGCA AGGTACGTGG CCTTTATTCC AGGCCAGAGC TCTCAGGGAG 2700
GAGCCTGGTG GATTTTGCCT CTGCTATTTT CTGGCTGTGT GACCTTGGGA AGACCACTTT 2760
ACTTCTCTGA TCTCCTGCAT CCTCAACTAG ATAATGCCTA CTACCCAAGG TTTACTAAAA 2820
GGACCAGGTG GCATGATGTC TGTGGGTGTG CTTTAGAAAC TGCAAAAAGT ACTGCAAAAG 2880
TGAGAGCTTG TCACCCCTGC ATCAGAGAGG CCCTAACACC AGGCCCTCTG GTCAGACAGC 2940
TTGCATCCGG TCGTGGCCCC ACCACATCCA ACCTGAGTGA CTTCGGGCAA GTGACTGAAC 3000
CTCTCTGAGC CTCAATTTTC TCATCTGCAA AATGGGACTG ATTATAGTAG CTATCACATA 3060