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

TagContent
EnhancerAtlas ID
HS093-00902 
Organism
Homo sapiens 
Tissue/cell
HL-60 
Coordinate
chr1:43400380-43401430 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr1:43400403-43400413GGCACGTGCC+6.02
HES2MA0616.2chr1:43400403-43400413GGCACGTGCC-6.02
RREB1MA0073.1chr1:43401030-43401050CCCCACACCACCTCCCGCCA+6.67
SPIBMA0081.2chr1:43401104-43401116CACTTCCCCTTT-6.07
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_01795chr1:43401101-43403350Aorta
SE_04284chr1:43399877-43402347Brain_Anterior_Caudate
SE_05390chr1:43400269-43403582Brain_Cingulate_Gyrus
SE_06192chr1:43395065-43405505Brain_Hippocampus_Middle
SE_07319chr1:43400813-43402381Brain_Hippocampus_Middle_150
SE_08269chr1:43400734-43404931Brain_Inferior_Temporal_Lobe
SE_10377chr1:43396392-43405534CD19_Primary
SE_11009chr1:43387831-43425728CD20
SE_12470chr1:43400220-43403900CD3
SE_12535chr1:43400610-43400723CD34_adult
SE_13825chr1:43400382-43401443CD34_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_23189chr1:43399749-43406265Colon_Crypt_1
SE_23904chr1:43400276-43401158Colon_Crypt_2
SE_23904chr1:43401192-43405387Colon_Crypt_2
SE_25177chr1:43399941-43405213Colon_Crypt_3
SE_26580chr1:43395721-43413249Esophagus
SE_29267chr1:43400819-43410293Fetal_Intestine_Large
SE_31882chr1:43401274-43405435Gastric
SE_34353chr1:43395339-43412997HCT-116
SE_35049chr1:43400682-43411164HeLa
SE_36013chr1:43400628-43405505HMEC
SE_39883chr1:43397369-43405479K562
SE_41620chr1:43399645-43401236LNCaP
SE_50202chr1:43396219-43406255Sigmoid_Colon
SE_54088chr1:43400594-43405374Spleen
SE_55821chr1:43399761-43405450u87
SE_57045chr1:43396858-43405413VACO_400
SE_58561chr1:43388242-43430420Ly1
SE_60624chr1:43388552-43428820DHL6
SE_62392chr1:43388423-43425814Tonsil
SE_64340chr1:43397259-43405516NHEK
SE_67781chr1:43399761-43405450u87
SE_68708chr1:43393050-43401454H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14340093243401203
Number: 1             
IDChromosomeStartEnd
GH01I042929chr14339554143414526
Enhancer Sequence
GGGTCATGTG TGAGGTGAGA CCTGGCACGT GCCTGTTCTG AACGCTCCCA CCTCACATGC 60
CCGTCCCAAG CTTAGGATTT AAACACTTGA TGCTGCCACC ACCCCACATC CATCCATCAC 120
CAGGTCCTCT CGATTCTGCC TCCGAGTCTG TCCTACTTCT CTACCCAGGC AGCCTGCCCT 180
GGGTCTCATC TGGATTCTGC TCCCGACTCT TCCTATCCAC CAAAGTCAGA CCCCATTTCC 240
CACAGTGAAC CACCCCTCAG AATGCAGTCG GAGTCCTGCA CACCAAATGT GCCAGGCTCG 300
GCCATCCACC CGCTTCTCTG CTCCCTTCCC AGCCCAGTCT CTTCACCCAG CTGTGGAGTC 360
TGGGTGGCGG CAAGCGTGTT GAGGAGGGAG GAGCGGTTCT GGTTAGTTCC TGGGGGGACT 420
GCCATGGTGT CGGCCAGCCT AGAGCTGAGG GGCTACTACA GATCTCTGTC CAGGTGCCTC 480
ACTGAGCCTA GAGGACACCC ACCATGGAGA CCACCCTGGA GAAGCAGGTT GACTCTGGGC 540
AGCTGAGATC CTTTGAACCG GATGGCTTCT GGTACGCGAA GCTATTCCTC ACCCGGTGGC 600
TCTCCTGGGG TGAGGGGGAG GCCTGCCCAA GCCTAAGGAC ACCTGGGAAT CCCCACACCA 660
CCTCCCGCCA GTCGAGGCAA CTGTGGGTGA GACTACATGT CTGCCCATCT GCCAAGGAAC 720
TTCTCACTTC CCCTTTGTAG AGGGGCATGA GGCGGCGAAC ACTGCCTGGC ACATGGGTAA 780
GCTGTTACTG CTGTCACTGT TGCTCTCTCA AGAAAAGAAG TCACCACTTT CGGAGGAGCC 840
TTAGGGACAA GGTTTTCCAT TTTGAAATTG CCAGAAATCA TTACCCTAAG AATGTAAGAG 900
TAAGGAGGAA CCTGAAGGAA CTACGGGCCT GCCTCAGGGA ATAAAGCTAG TCTCCAGACC 960
CTGCTCGGCT GCTCCTGGCA GAGGAACCCA GCACTCTGTA GCCCCAGAGG GCAGAGGTGC 1020
CAGGGCCAGA CTCCAGCTCA GGGGAAGGAA 1050