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

TagContent
EnhancerAtlas ID
HS026-08858 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr12:124853760-124856560 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFICMA0161.2chr12:124853805-124853816TCTGCCAAGAA-6.02
SRFMA0083.3chr12:124855929-124855945TGACCTTATTTGGAAA-6.01
TFAP2CMA0524.2chr12:124855566-124855578AGCCCCAGGGCA+6.11
ZBTB18MA0698.1chr12:124855136-124855149CATCCAGATGTGA+6.07
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00866chr12:124852302-124857914Adrenal_Gland
SE_02192chr12:124852573-124855748Aorta
SE_02420chr12:124853362-124855303Astrocytes
SE_03150chr12:124852582-124854142Brain_Angular_Gyrus
SE_03150chr12:124854154-124855845Brain_Angular_Gyrus
SE_03868chr12:124852326-124856486Brain_Anterior_Caudate
SE_04770chr12:124852265-124856998Brain_Cingulate_Gyrus
SE_05769chr12:124851534-124858012Brain_Hippocampus_Middle
SE_06714chr12:124852249-124856790Brain_Hippocampus_Middle_150
SE_07720chr12:124852393-124856669Brain_Inferior_Temporal_Lobe
SE_23639chr12:124852547-124855286Colon_Crypt_1
SE_24091chr12:124853655-124854883Colon_Crypt_2
SE_25142chr12:124853624-124855051Colon_Crypt_3
SE_26654chr12:124852402-124856810Esophagus
SE_28184chr12:124853346-124855413Fetal_Intestine
SE_29418chr12:124853184-124855403Fetal_Intestine_Large
SE_29559chr12:124852384-124855597Fetal_Muscle
SE_31405chr12:124852239-124857127Gastric
SE_38211chr12:124852268-124855751HUVEC
SE_40749chr12:124851606-124856969Left_Ventricle
SE_41561chr12:124852351-124857884LNCaP
SE_42183chr12:124852349-124856857Lung
SE_44453chr12:124852334-124855577NHDF-Ad
SE_45099chr12:124853338-124855555NHLF
SE_46642chr12:124852508-124855752Ovary
SE_46642chr12:124855953-124856916Ovary
SE_47406chr12:124852344-124856831Panc1
SE_47472chr12:124853387-124855312Pancreas
SE_48155chr12:124851582-124857802Psoas_Muscle
SE_48612chr12:124852376-124856560Right_Atrium
SE_49559chr12:124852544-124855378Right_Ventricle
SE_50109chr12:124852450-124856867Sigmoid_Colon
SE_51247chr12:124852084-124856783Skeletal_Muscle
SE_52804chr12:124852392-124856729Small_Intestine
SE_54428chr12:124853228-124855766Spleen
SE_54615chr12:124852448-124855767Stomach_Smooth_Muscle
SE_65244chr12:124852447-124857871Pancreatic_islets
Number: 1             
IDChromosomeStartEnd
GH12I124367chr12124851691124856859
Enhancer Sequence
CAGGCAGGCT CGGGGTTTTG CAATTGAAGC CACTATCTCT GGTCGTCTGC CAAGAAAACA 60
CCCAGGCAGA GCCACCTCGA AGAAAGTGCC AGCGGGCCGA AGGAGAATGT GATTTTCTCT 120
CTCCCAAAGT CACCGGGGCG GGGGGCCAGA TGAGAGTCAT CTTGCGTCCA TCCAGGAACA 180
CAGAGCTCCC CCACTGGGGC TGCCAGGCAG GAGGGATGAT ACTGGGCGGG CAGCCAGGAG 240
CAGGGGTCGC CTGGGGGGCC CGCCCGTCCC ACCAGCCCTT CCCGGGAGGC CCTGGCTGCC 300
AGGGCCTACT CTGACGCATC TCGTCCGCGT CCTCCAGCGT CCGCCCGGCC CTGCGCAGTC 360
GTGGCCGGCA GAGGGAGGGG TGGCGGGCTG CCGGCCAGGA CGAGGTCAGC AGGCTGGCCA 420
GAGTCCAGCC TCGTTCACTG AGAGGGCAAA GCAGGCCCCA AGGGCGGGGG CCTGGGCCTA 480
GTCGCACAGG GCGGGACAAA CCAGGTGTCC TGACTCCCAG CCGAGGACTC CTGCACCCGG 540
GGGCTGTGTG CTGGACACTG GGCAAGGGGT GGACGTACGC CAGGCCCAGC TCGGGGAGGG 600
AGGACACGGC CCTGGGCGGG GCTGCAGGGG AGAGGACGGG AGGCTGCAAG TGCCCTGCGG 660
GGCCTCAGGC CTAGCCTGAG TGTTCTGGGG ACGGACAGGA TGCAAGCTGA TCCCCCGGCT 720
CCCCAGTCCG GGGCCAGCCA CATGGACCCA AAATACAGAC TCTGGGAGGC AGCTTATCAA 780
TGGGGCTGCC CCATGACCTC AGCGGTCCCC CGGCGAAGGC AGAAACATGT GTTTCTATGA 840
CTCTGTCCCC ACAGCCAGCA GGAGCGGGGC GGGGAGCCGT CTGCCCTGAC CCCGCTATCC 900
AGGCACAATG GCCCTGGCTG CCTGCCTCCA GGGCAGACCC AGCCACACCA TGAACACTGT 960
TTTCCAAGCT GGGACTGTCG GGCAAGAAGC TCAGGGATTT GGTGCCCTCA GAAACCCGCA 1020
GGCCAGGCCT TTGCTCATCA CAGGGTCAGG GTCAGGCCGT CCACTTCTCA CACGCATGGG 1080
CGCGGTTCCT GTTGGCAGTG GTTCCTGGGG ACCCTGAGAT TTTGTTTTGT GGAACCTATA 1140
GAGATCCGGG TGAACCTCAG TTCCTAGGGA ATGTCCTAGG ACTTCCCCCT TTAACATGGC 1200
CCAGGGTGAA CCCCAGGGCA GAGACAAGGG CCCCGCATGA CCCTGCGGGT CTGATTTTCC 1260
TCCCTCGCTT GCTCTGCCCA GGACCATTCC AAGGGACTTG GGAGGGGAGA AAACAGACCA 1320
CACTGTAGTT GAAATAAAAT GGCCTGCCTG CCCCACCAGA AAACAATTCC TCCAGCCATC 1380
CAGATGTGAG CAGGACGCAG TCTCCGCGGG TCTGCCCTCT GCCAACCGAG ATTGGCCCTA 1440
ACTTGGGTAG CCATCTTTGG TTCTGGGCTG GAGGCCTTGA GGCCCAAAGC ATCTGTGCTG 1500
AAAATGGGTA AAAGGTGGCA TTCTCAGGGA TGTGGGGTCA CCCAGGCCAG GAGCAAAGAC 1560
AGAGGCCAGA AAGGAAAGAA CACACCTCAG AGACATCAAC ACCCAAACAG GACGACACTG 1620
GGGTCCTCCA GGCCACCCCA GCTGGAGAGG AATTTGCAAG GGGAACCTCT GCACCTGTGA 1680
TCCAAGGTGA TCACCTGTGA TCCTGAGCCC TGGACCCTTG GCTGATGGGA GATGAGCCAC 1740
CAAAAACATG TTGAACCTGT GGCTTTTCCC CAACCCCACG GCCACCACGC TCGCATCTCC 1800
ATCACCAGCC CCAGGGCACT TGCAGCTGCC TCCTGACTGT GCCTCTCACT CCCAGCAAAT 1860
CCCCCACATG GTTTCATGGG TAAATCACAT CTGGCTCTCT TGGGAGAGGC TCGTAAAGGC 1920
CTTCTCACTG CCCTGAGAAC AAAATGCAGC CCCCACCTGC CAGGGCGTGA CTCAGTGCCC 1980
CCACCCCCGT GAGAGCTGCC CCCCGTCCTG CCAGGCTGCC CCCTCCCTGA GCCACCCTTT 2040
GGCACCTGAA TCCACCAAGC TCATTCCCAC CTCGGGCCTT CGCACTTGCT GTTCCCACCA 2100
CGCTGAGGGT AGAACTGTGT CCCCCCAGAG AAGGTACATT CAAGTCCTAA CCCAGGGTCT 2160
CTGTGAATGT GACCTTATTT GGAAATAGAC TGTTTGCTGA TATAATCAAG TTAAGATGAA 2220
GCTGCACTAG ATTAGGACAG CTGCCCATCC AATGCCTGGT GTCCTCAGAA GAAGAAAGTG 2280
TGGACACAGA GATGCACAGG GCGAAGGTCA TGTGACAGCA GAGCCAAAGA CGGAGTGGCA 2340
TGCCAGCAAT CACGACCGCC AGCAGCGGCC AGGAGCTGGA AGAGGCGGGA TGGATCTGCC 2400
CAGAGGCTCG GAGGCTGCGT CTCGGCCTGC ATGGTGCCCC CAGGCTCCTG GCCTCCAGGA 2460
CTGTATTTGT TAAAAGCCAC CTGGCTCGAA CTACCTTGTG AGGGCGGCCC TAGGAAGCGA 2520
GCAGGCTGCC TGGCACACTC TCTCCCTAGC GCTGCCCAGG GCTGCCTCCT CTGTCCGGGT 2580
CTCAGCTTGG ATGTCACCTC CTGGGGAGGT CCTCCCGGCC ACACCTCCGC CCCTTCCTGG 2640
CCTGCATCTC TCATTCCTGG ACTCTACTCC AAGTCTGCCT CCCTAACCAC ACCTCGGGCT 2700
CCCCCAAAGC AGGCAGAGCC AGACTGGGTG CGGCTGTCTA AGTAGGTAGT CGCTGCTCAG 2760
TGTCTGCAGA CAAAAGCCAA GGTTAGGGCT GCCTGGCGCC 2800