EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-01493 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr1:43397330-43398920 
Target genes
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
TACTAAAAAT AAAAAAAAAA TTAGCTGGAC GTGGTGGCGC AAGCATGTAA TCCCAGCTAC 60
ACGGGAGGCT AAGGCAGAAT TGCTTAAACC CAGGACACGG AGTTTGCAGT GAGCCAAGAC 120
TGTGCCACTG CACTTCAGCC TGAGTGACAG AGTGAGACTC TATGTCTCAA AAAAAAAAAA 180
AAAAAAAGAG AAATACAGAA GGAAAAGGGT CTTCCCACTT GCCCCTTTTC TCCTCACCAT 240
GTCTCAAAGC CCCAGGGGCC CATCTCCTGC CATCAGGCCC TCCCCCCAAC CCCTTGCTGG 300
GGAGGAAGCA GGGCTTGACA GACAGGTTCC GCCATCCAGG AAGTACAGAC TCCCTGACCG 360
CACTGAGGGC CTGGTGTGAC AAACTCACAC ATGTCACCCT TCAGAAGTGC TTGAAAGACT 420
CACGCTGTGG CTTTCTGTTC CCCAGGCCTA GCTCCCTTGT GTCTGGCCTG CGAGCACCCC 480
CTTGAAGGAC CCACGGCCTC CTCCCCTCTC CCAAGGGCCC AGCTAGGAGG TATGGGGAAA 540
GGTTCCACAC AAGGAAGCAG TTCCAGGAAC TGGAAACGCC CGTCCTAGGG CAGCCCTGCC 600
CACCAGCCCT GCCCCCACCC TGGCCAGCTC CCACGGATGT GGTAGGCAGG CAGCACCCGT 660
TCTGCCTGAG CACACTCACC ACACTCTCAG TGCCATGGGA CTGGCCAGAC CCACCCAGCC 720
ACACGTATAG CAGAGTGCAG GCCCTAGTTA CCCAGAAACG GCTTCTTATG CACGTATACC 780
ATCACACACA CATACCCGTG CTCATAGAAT CTAAATATTC CTGCTTTAGC CAGTCACAAA 840
CTCACATGCC CCTCATCCCC TACCACTTAC AGCTCAAACT CAATTCCATG TGAACCCAAC 900
CCATCCCAAC ACCCCTCCGT GTGTGTGCAT GCCACAGGTT CATGCACACA CAGCGGTATG 960
CAGCCTCTGC AGCCTCCATC ACTGCTGTTG GTCCTCCCTA TCCCTTCCAA CCCACTGAGG 1020
TCTAGCAGAA GAAGAAGGTG TGGGCAGGCA CACTTGCCAA ACCAAAGCCT GCAGTCCCAG 1080
AAATGCCCAC CTATTCAAAT ATGCTGGGCC TGCCTCCTGG TGCCTTCCTT CCCATTGCTG 1140
TGGGTGCTCA GCCTCTAGCC ATCTTTTCCC CTGCCCTGTC ACAACCTGTC CCAAGTCAGC 1200
AGGCATCTGA TGGAGGCCAG GCTCCAAGGG GCGAGGACAG TTGGTAGGGC AGAGGCAAGC 1260
CCTAAGGATC TGCTTGTCCG TTCCAAGGAC GCCATGCAGG GCAGTGAATA GAAACCTGAA 1320
CTCTGATTCT GGACACAACT AAATTCAGGT CCTAGCTCCA CCCCTTATTT CCAGTGTGAC 1380
CATGAGCAAG TTATTTCATC TGTGAGTTTC CATGGCCCCA TTTCTAAAGT GCAGACATTA 1440
GCAGGAGCTG CTTCACAGTG CTGCAGGGAA TCAGTGAAAC AGTGCTTGGT GTCATCATCC 1500
CTAAAATCAC CCCACTGCAC ACTGGTGGCC TGAAGGCTGT GCAGACCACT AACAGAGTCT 1560
CCCCAAGCCT TCAACCCGTA ACTCAAAATC 1590