EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS158-01700 
Organism
Homo sapiens 
Tissue/cell
Pancreas 
Coordinate
chr1:43397380-43399010 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MYBMA0100.3chr1:43398565-43398575GACAGTTGGT-6.02
RREB1MA0073.1chr1:43398223-43398243ACCCAACCCATCCCAACACC+6.09
SREBF1MA0595.1chr1:43398835-43398845ATCACCCCAC+6.02
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_01795chr1:43397398-43398157Aorta
SE_05390chr1:43397289-43399585Brain_Cingulate_Gyrus
SE_06192chr1:43395065-43405505Brain_Hippocampus_Middle
SE_07319chr1:43396705-43398566Brain_Hippocampus_Middle_150
SE_08269chr1:43397488-43399602Brain_Inferior_Temporal_Lobe
SE_10377chr1:43396392-43405534CD19_Primary
SE_11009chr1:43387831-43425728CD20
SE_12470chr1:43397348-43399808CD3
SE_13825chr1:43396778-43399313CD34_Primary_RO01536
SE_14471chr1:43395753-43414527CD4_Memory_Primary_7pool
SE_19657chr1:43396427-43405202CD4p_CD25-_Il17p_PMAstim_Th17
SE_20345chr1:43395492-43405550CD56
SE_20799chr1:43396312-43405729CD8_Memory_7pool
SE_22754chr1:43395674-43405513CD8_primiary
SE_23189chr1:43397346-43399720Colon_Crypt_1
SE_23904chr1:43397399-43399265Colon_Crypt_2
SE_25177chr1:43396926-43398787Colon_Crypt_3
SE_26580chr1:43395721-43413249Esophagus
SE_29267chr1:43397108-43398616Fetal_Intestine_Large
SE_31882chr1:43396701-43399114Gastric
SE_33837chr1:43396695-43400408HCC1954
SE_34353chr1:43395339-43412997HCT-116
SE_36013chr1:43398145-43399517HMEC
SE_37191chr1:43393285-43398371HSMMtube
SE_39883chr1:43397369-43405479K562
SE_41620chr1:43397520-43399349LNCaP
SE_42796chr1:43396336-43399368Lung
SE_50202chr1:43396219-43406255Sigmoid_Colon
SE_54088chr1:43396020-43399837Spleen
SE_55340chr1:43396132-43399459Thymus
SE_55821chr1:43396763-43399673u87
SE_57045chr1:43396858-43405413VACO_400
SE_57417chr1:43397518-43398729VACO_503
SE_58269chr1:43397518-43398137VACO_9m
SE_58561chr1:43388242-43430420Ly1
SE_60624chr1:43388552-43428820DHL6
SE_62392chr1:43388423-43425814Tonsil
SE_64094chr1:43397486-43398043HSMM
SE_64340chr1:43397259-43405516NHEK
SE_67781chr1:43396763-43399673u87
SE_68708chr1:43393050-43401454H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14339760043398000
Number: 1             
IDChromosomeStartEnd
GH01I042929chr14339554143414526
Enhancer Sequence
TCCCAGCTAC ACGGGAGGCT AAGGCAGAAT TGCTTAAACC CAGGACACGG AGTTTGCAGT 60
GAGCCAAGAC TGTGCCACTG CACTTCAGCC TGAGTGACAG AGTGAGACTC TATGTCTCAA 120
AAAAAAAAAA AAAAAAAGAG AAATACAGAA GGAAAAGGGT CTTCCCACTT GCCCCTTTTC 180
TCCTCACCAT GTCTCAAAGC CCCAGGGGCC CATCTCCTGC CATCAGGCCC TCCCCCCAAC 240
CCCTTGCTGG GGAGGAAGCA GGGCTTGACA GACAGGTTCC GCCATCCAGG AAGTACAGAC 300
TCCCTGACCG CACTGAGGGC CTGGTGTGAC AAACTCACAC ATGTCACCCT TCAGAAGTGC 360
TTGAAAGACT CACGCTGTGG CTTTCTGTTC CCCAGGCCTA GCTCCCTTGT GTCTGGCCTG 420
CGAGCACCCC CTTGAAGGAC CCACGGCCTC CTCCCCTCTC CCAAGGGCCC AGCTAGGAGG 480
TATGGGGAAA GGTTCCACAC AAGGAAGCAG TTCCAGGAAC TGGAAACGCC CGTCCTAGGG 540
CAGCCCTGCC CACCAGCCCT GCCCCCACCC TGGCCAGCTC CCACGGATGT GGTAGGCAGG 600
CAGCACCCGT TCTGCCTGAG CACACTCACC ACACTCTCAG TGCCATGGGA CTGGCCAGAC 660
CCACCCAGCC ACACGTATAG CAGAGTGCAG GCCCTAGTTA CCCAGAAACG GCTTCTTATG 720
CACGTATACC ATCACACACA CATACCCGTG CTCATAGAAT CTAAATATTC CTGCTTTAGC 780
CAGTCACAAA CTCACATGCC CCTCATCCCC TACCACTTAC AGCTCAAACT CAATTCCATG 840
TGAACCCAAC CCATCCCAAC ACCCCTCCGT GTGTGTGCAT GCCACAGGTT CATGCACACA 900
CAGCGGTATG CAGCCTCTGC AGCCTCCATC ACTGCTGTTG GTCCTCCCTA TCCCTTCCAA 960
CCCACTGAGG TCTAGCAGAA GAAGAAGGTG TGGGCAGGCA CACTTGCCAA ACCAAAGCCT 1020
GCAGTCCCAG AAATGCCCAC CTATTCAAAT ATGCTGGGCC TGCCTCCTGG TGCCTTCCTT 1080
CCCATTGCTG TGGGTGCTCA GCCTCTAGCC ATCTTTTCCC CTGCCCTGTC ACAACCTGTC 1140
CCAAGTCAGC AGGCATCTGA TGGAGGCCAG GCTCCAAGGG GCGAGGACAG TTGGTAGGGC 1200
AGAGGCAAGC CCTAAGGATC TGCTTGTCCG TTCCAAGGAC GCCATGCAGG GCAGTGAATA 1260
GAAACCTGAA CTCTGATTCT GGACACAACT AAATTCAGGT CCTAGCTCCA CCCCTTATTT 1320
CCAGTGTGAC CATGAGCAAG TTATTTCATC TGTGAGTTTC CATGGCCCCA TTTCTAAAGT 1380
GCAGACATTA GCAGGAGCTG CTTCACAGTG CTGCAGGGAA TCAGTGAAAC AGTGCTTGGT 1440
GTCATCATCC CTAAAATCAC CCCACTGCAC ACTGGTGGCC TGAAGGCTGT GCAGACCACT 1500
AACAGAGTCT CCCCAAGCCT TCAACCCGTA ACTCAAAATC GGGGCTCCTG CCAGGTATCA 1560
ATCCAATCTC CCTACCTACC ACACCTTTGC ACTCACTACA CACCATCTCC CACCCCTCTA 1620
CGCCTTTGAG 1630